Coleoptera (Order)
Related Symbionts
577 recordsSymbiont records associated with Coleoptera order
Classification | Host | Function | Function Tags | Reference | |
---|---|---|---|---|---|
Rhodobacter
Pseudomonadota |
Bacteria
|
Rhodanobacter genera can utilize various carbon sources, including cellobiose. In larvae of longhorned beetles that feed on plants rich in carbohydrates (cellulose and hemicellulose) and lignin, Rhodanobacter can help the larvae digest more carbon nutrients through carbon sequestration |
Digestive enzymes
|
||
Candidatus Ishikawaella capsulata
Pseudomonadota |
Bacteria
|
Laboratory-reared and field-collected P. chrysocephala all contained three core genera Pantoea, Acinetobacter and Pseudomonas, and reintroduction of Pantoea sp. Pc8 in antibiotic-fed beetles restored isothiocyanate degradation ability in vivo (by 16S rRNA gene sequencing and LC-MS) |
Plant secondary metabolites
|
||
Pantoea sp. Pc8
Pseudomonadota |
Bacteria
|
Laboratory-reared and field-collected P. chrysocephala all contained three core genera Pantoea, Acinetobacter and Pseudomonas, and reintroduction of Pantoea sp. Pc8 in antibiotic-fed beetles restored isothiocyanate degradation ability in vivo (by 16S rRNA gene sequencing and LC-MS) |
Plant secondary metabolites
|
||
Methylovirgula
Pseudomonadota |
Bacteria
|
Methylovirgula is ubiquitous in soil and has been found in many soil samples as a major species producing carbon activity, scholars have found that the microorganism has the highest content in mixed peat swamp forest systems and has the effect of harnessing and reducing methane |
- | ||
Staphylococcus gallinarum
Bacillota |
Bacteria
|
The strain encodes complete biosynthetic pathways for the production of B vitamins and amino acids, including tyrosine; A carbohydrate-active enzyme search revealed that the genome codes for a number of digestive enzymes, reflecting the nutritional ecology of C. maculatus |
Nutrient provision
Digestive enzymes
|
||
Burkholderia gladioli
Pseudomonadota |
Bacteria
|
process a cryptic gene cluster that codes for the biosynthesis of a novel antifungal polyketide with a glutarimide pharmacophore, which led to the discovery of the gladiofungins as previously-overlooked components of the antimicrobial armory of the beetle symbiont |
Antimicrobials
|
||
Serratia bockelmannii
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia bockelmannii
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia bockelmannii
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. PF2-63
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. PF-27
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-PFBMAAmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-PFBMAAmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-PFBMAAmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-RSBMAAmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-RSBMAAmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-RSBMAAmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-RSmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-RSmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Serratia sp. Se-RSmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Stenotrophomonas sp. PFBMAA-4
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Stenotrophomonas sp. RS-48
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Stenotrophomonas sp. St-PFBMAAmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Stenotrophomonas sp. St-PFmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Stenotrophomonas sp. St-RSBMAAmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Stenotrophomonas sp. St-RSmG
Pseudomonadota |
Bacteria
|
suggesting the occurrence of an unprecedented desferrioxamine-like biosynthetic pathway,including desferrioxamine B, which may help tolerating diets rich in azoxyglycosides, BMAA, and other cycad toxins, including a possible role for bacterial siderophores |
Plant secondary metabolites
|
||
Monacrosporium ambrosium
Ascomycota |
Fungi
|
provides not only the food and sterol skeleton necessary for the development of the beetle during its larval stages, but also serves as a producer of fungal inhibitors pigmented naphthoquinones that help to preserve the purity of the fungal garden of host |
Nutrient provision
Antimicrobials
Fungal farming
|
||
Pseudomonas sp. 7 B321
Pseudomonadota |
Bacteria
|
volatiles from predominant bacteria regulate the consumption sequence of carbon sources d-pinitol and d-glucose in the fungal symbiont Leptographium procerum, and appear to alleviate the antagonistic effect from the fungus against RTB larvae |
- | ||
Rahnella aquatilis B3None1
Pseudomonadota |
Bacteria
|
volatiles from predominant bacteria regulate the consumption sequence of carbon sources d-pinitol and d-glucose in the fungal symbiont Leptographium procerum, and appear to alleviate the antagonistic effect from the fungus against RTB larvae |
- | ||
Serratia liquefaciens B31None
Pseudomonadota |
Bacteria
|
volatiles from predominant bacteria regulate the consumption sequence of carbon sources d-pinitol and d-glucose in the fungal symbiont Leptographium procerum, and appear to alleviate the antagonistic effect from the fungus against RTB larvae |
- | ||
Acinetobacter sp.
Pseudomonadota |
Bacteria
|
Acinetobacter sp. in C. chinensis enriched after treating with saponin, and when incubating bacteria with saponin for 72 h, saponin content significantly decreased from 4.054 to 1.867 mg/mL (by 16S rRNA metagenome sequencing and HPLC) |
Plant secondary metabolites
|
||
Pseudomonas fulva
Pseudomonadota |
Bacteria
|
Antibiotic-treated larvae showed lower caffeine-degrading activity and increased mortality. These deficients were recovered by inoculation of the caffeine-degrading symbiont. A caffeine-degrading gene was detected from the symbiont |
Plant secondary metabolites
|
||
Candidatus Stammera capleta
Pseudomonadota |
Bacteria
|
Insect hosts depend on symbiont to degrade pectin;the symbiont nonetheless retained a functional pectinolytic metabolism targeting the polysaccharide's two most abundant classes: homogalacturonan and rhamnogalacturonan I |
- | ||
Serratia harmoniae
Pseudomonadota |
Bacteria
|
the harlequin ladybird safely harbors Serratia harmoniae, a highly pathogenic bacterium that causes severe mortality in other ladybird species, which confers an intraguild predation advantage to the harlequin ladybird |
Natural enemy resistance
|
||
Burkholderia gladioli
Pseudomonadota |
Bacteria
|
the symbionts inhibit the growth of antagonistic fungi on the eggs of the insect host, indicating that the Lagria-associated Burkholderia have evolved from plant pathogenic ancestors into insect defensive mutualists |
Antimicrobials
|
||
Burkholderia gladioli
Pseudomonadota |
Bacteria
|
the symbionts inhibit the growth of antagonistic fungi on the eggs of the insect host, indicating that the Lagria-associated Burkholderia have evolved from plant pathogenic ancestors into insect defensive mutualists |
Antimicrobials
|
||
Leptographium procerum
Ascomycota |
Fungi
|
enhances the survivorship and overall fitness of invasive beetles by degrading the host phenolic naringenin, ultimately overcoming the tree defenses and facilitating the success of the invasive beetle-Fungi complex |
Plant secondary metabolites
|
||
Burkholderia
Pseudomonadota |
Bacteria
|
It can trongly degrade naringenin, and pinitol, the main soluble carbohydrate of P. tabuliformis, is retained in L. procerum-infected phloem and facilitate naringenin biodegradation by the microbiotas. |
Digestive enzymes
|
||
Novosphingobium
Pseudomonadota |
Bacteria
|
It can trongly degrade naringenin, and pinitol, the main soluble carbohydrate of P. tabuliformis, is retained in L. procerum-infected phloem and facilitate naringenin biodegradation by the microbiotas. |
Digestive enzymes
|
||
Rhodotorula
Basidiomycota |
Fungi
|
It can trongly degrade naringenin, and pinitol, the main soluble carbohydrate of P. tabuliformis, is retained in L. procerum-infected phloem and facilitate naringenin biodegradation by the microbiotas. |
Digestive enzymes
|
||
Grosmannia clavigera
Ascomycota |
Fungi
|
Grosmannia clavigera can detoxify oleoresin terpenoids (conifer-defence chemicals) and utilize them as carbon sources. It allows host insects to tolerate terpenoids and grow successfully on pine hosts |
Plant secondary metabolites
|
||
Candidatus Shikimatogenerans silvanidophilus
Bacteroidota |
Bacteria
|
the symbionts accelerate their host's cuticle formation and thereby enable it to quickly reach a cuticle quality threshold that confers structural protection against predation and fungal infection |
- | ||
Raffaelea lauricola
Ascomycota |
Fungi
|
Volatile cues from fungal symbionts may function as a mechanism to locate established fungal gardens of conspecific beetles (suitable microhabitat) but also as an orientation cue within a gallery |
Fungal farming
|
||
Burkholderia gladioli
Pseudomonadota |
Bacteria
|
Bacteria produce icosalide, an unusual two-tailed lipocyclopeptide antibiotic,which is active against entomopathogenic bacteria, thus adding to the chemical armory protecting beetle offspring |
Antimicrobials
|
||
Pseudomonas fulva
Pseudomonadota |
Bacteria
|
P. fulva processed gene coding one subunit of caffeine demethylase, and reinstatement of P. fulva in germ-free H. hampei degraded all caffeine consumed (by 16S rRNA gene sequencing and GC-MS) |
Plant secondary metabolites
|
||
Yarrowia-like yeast BNone2
Ascomycota |
Fungi
|
potentially facilitate carcass utilization by producing digestive enzymes, eliminating cadaver-associated toxic volatiles, and releasing antimicrobials to sanitize the microenvironment |
Digestive enzymes
Antimicrobials
|
||
Yarrowia-like yeast C11
Ascomycota |
Fungi
|
potentially facilitate carcass utilization by producing digestive enzymes, eliminating cadaver-associated toxic volatiles, and releasing antimicrobials to sanitize the microenvironment |
Digestive enzymes
Antimicrobials
|
||
Yarrowia-like yeast ENone2
Ascomycota |
Fungi
|
potentially facilitate carcass utilization by producing digestive enzymes, eliminating cadaver-associated toxic volatiles, and releasing antimicrobials to sanitize the microenvironment |
Digestive enzymes
Antimicrobials
|
||
Shikimatogenerans bostrichidophilus
Bacteroidota |
Bacteria
|
encodes the shikimate pathway to produce tyrosine precursors in its severely reduced genome, likely supplementing the beetles’ cuticle biosynthesis, sclerotisation, and melanisation. |
Nutrient provision
|
||
Lactococcus lactis
Bacillota |
Bacteria
|
contribute to the decomposition of complex carbohydrates, fatty acids, or polysaccharides in the insect gut. It might also contribute to the improvement of nutrient availability. |
Digestive enzymes
Nutrient provision
|
||
Hesperomyces harmoniae
Ascomycota |
Fungi
|
female ladybirds co-infected with Hesperomyces harmoniae and Spiroplasma had a significantly lower fecundity and hatchability compared to females with only one or no symbiont |
Reproductive manipulation
|
||
Spiroplasma
Mycoplasmatota |
Bacteria
|
female ladybirds co-infected with Hesperomyces harmoniae and Spiroplasma had a significantly lower fecundity and hatchability compared to females with only one or no symbiont |
Reproductive manipulation
|
||
Bostrichicola ureolyticus
Bacteroidota |
Bacteria
|
complement the function of Shikimatogenerans by recycling urea and provisioning the essential amino acid lysine, thereby providing additional benefits on nitrogen-poor diets |
Nutrient provision
|
||
Lactococcus
Bacillota |
Bacteria
|
were predicted to have genes related to hydrocarbon, fatty acids, and chitin degradation, which may assist their hosts in digesting the wax shell covering the scale insects |
Digestive enzymes
|
||
Sodalis pierantonius
Pseudomonadota |
Bacteria
|
endosymbiont dynamics parallels numerous transcriptional changes in weevil developing adults and affects several biological processes, including metabolism and development |
Growth and Development
|
||
Acinetobacter
Pseudomonadota |
Bacteria
|
These bacterial phyla may allow the adults C. maculatus to survive on DDVP treated grains, thereby making it inappropriate to control the beetle populations in the field. |
Pathogen interaction
|
||
Citrobacter
Pseudomonadota |
Bacteria
|
These bacterial phyla may allow the adults C. maculatus to survive on DDVP treated grains, thereby making it inappropriate to control the beetle populations in the field. |
Pathogen interaction
|
||
Bacteria
|
These bacterial phyla may allow the adults C. maculatus to survive on DDVP treated grains, thereby making it inappropriate to control the beetle populations in the field. |
Pathogen interaction
|
|||
Pseudomonas
Pseudomonadota |
Bacteria
|
These bacterial phyla may allow the adults C. maculatus to survive on DDVP treated grains, thereby making it inappropriate to control the beetle populations in the field. |
Pathogen interaction
|
||
Graphium euwallaceae
Ascomycota |
Fungi
|
G. euwallacea is the predominant symbiont in the initial stages of gallery formation and the main food source (i.e., dominant fungus) for larvae during their development |
Fungal farming
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
show a strong inhibitory activity against entomopathogenic Beauveria bassiana by reducing the fungal conidial germination and growth rather than regulating host immunity |
Antimicrobials
|
||
Serratia
Pseudomonadota |
Bacteria
|
show a strong inhibitory activity against entomopathogenic Beauveria bassiana by reducing the fungal conidial germination and growth rather than regulating host immunity |
Antimicrobials
|
||
Endoconidiophora polonica
Ascomycota |
Fungi
|
volatile compounds produced by Fungi may act as recognition signals for bark beetles to maintain specific microbial communities that might have impact on their fitness |
Chemical biosynthesis
|
||
Enterobacteriaceae bacterium F1
Pseudomonadota |
Bacteria
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum) |
Plant defense
|
||
Enterobacter sp. S1
Pseudomonadota |
Bacteria
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum) |
Plant defense
|
||
Enterobacter sp. T1
Pseudomonadota |
Bacteria
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum) |
Plant defense
|
||
Grosmannia europhioides
Ascomycota |
Fungi
|
volatile compounds produced by Fungi may act as recognition signals for bark beetles to maintain specific microbial communities that might have impact on their fitness |
Chemical biosynthesis
|
||
Grosmannia penicillata
Ascomycota |
Fungi
|
volatile compounds produced by Fungi may act as recognition signals for bark beetles to maintain specific microbial communities that might have impact on their fitness |
Chemical biosynthesis
|
||
Ophiostoma bicolor
Ascomycota |
Fungi
|
volatile compounds produced by Fungi may act as recognition signals for bark beetles to maintain specific microbial communities that might have impact on their fitness |
Chemical biosynthesis
|
||
Ophiostoma piceae
Ascomycota |
Fungi
|
volatile compounds produced by Fungi may act as recognition signals for bark beetles to maintain specific microbial communities that might have impact on their fitness |
Chemical biosynthesis
|
||
Pseudomonas sp. B1
Pseudomonadota |
Bacteria
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum) |
Plant defense
|
||
Pseudomonas sp. I2
Pseudomonadota |
Bacteria
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum) |
Plant defense
|
||
Raoultella sp. L1
Pseudomonadota |
Bacteria
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum) |
Plant defense
|
||
Sphingobacterium sp. N1
Bacteroidota |
Bacteria
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum) |
Plant defense
|
||
Stenotrophomonas sp. A3
Pseudomonadota |
Bacteria
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum) |
Plant defense
|
||
Burkholderia
Pseudomonadota |
Bacteria
|
be commonly found in plant roots and they all have nitrogen fixation abilities,and may be able to trigger the expression of genes associated with disease resistance |
Plant defense
|
||
Leptographium procerum CMW25626
Ascomycota |
Fungi
|
consumption of one common carbon source d-glucose over another carbohydrate d-pinitol in pine phloem tissues by the fungus inhibit D. valens larval weight increase |
Growth and Development
|
||
Klebsiella oxytoca
Pseudomonadota |
Bacteria
|
Antibiotic-treated larvae suffered growth retardation on a diet containing plant extract or swainsonine. Gut bacteria showed toxin-degradation activities in vitro |
Plant secondary metabolites
|
||
Pantoea 1C4
Pseudomonadota |
Bacteria
|
plays both a nutritional role, by providing essential amino acids and enzymes for the hydrolysis of plant biomass, and a defensive role, by producing antibiotics. |
Nutrient provision
Antimicrobials
|
||
Pantoea 1C4
Pseudomonadota |
Bacteria
|
plays both a nutritional role, by providing essential amino acids and enzymes for the hydrolysis of plant biomass, and a defensive role, by producing antibiotics. |
Nutrient provision
Antimicrobials
|
||
Pseudomonas aeroginosa
Pseudomonadota |
Bacteria
|
Antibiotic-treated larvae suffered growth retardation on a diet containing plant extract or swainsonine. Gut bacteria showed toxin-degradation activities in vitro |
Plant secondary metabolites
|
||
Sitophilus oryzae principal endosymbiont (SOPE)
Pseudomonadota |
Bacteria
|
induces the specific differentiation of the bacteriocytes, increases mitochondrial oxidative phosphorylation through the supply of pantothenic acid and riboflavin |
Nutrient provision
|
||
Bacteroidetes
Bacteroidota |
Bacteria
|
Affect cuticle thickness, melanization and hydrocarbon profile, enhancing desiccation resistance and thereby strongly improving fitness under dry conditions. |
- | ||
Enterobacter BC-8
Pseudomonadota |
Bacteria
|
symbiotic bacteria suppressed plant defenses such as hydrogen peroxide and phenolic compounds accumulation and activity of peroxidases and trypsin inhibitors |
Plant defense
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
Wolbachia harbored dominantly in a female than the male adult, while, no significant differences were observed between male and female body parts and tissues |
- | ||
Bacteroidia
Bacteroidota |
Bacteria
|
affect cuticle thickness, melanization and hydrocarbon profile, enhancing desiccation resistance and thereby strongly improving fitness under dry conditions |
- | ||
Grosmannia clavigera
Ascomycota |
Fungi
|
The symbiotic fungus can utilize terpenes as carbon sources. Genes involved in terpene-degradation were expressed in symbionts cultured with plant materials |
Digestive enzymes
|
||
Grosmannia europhioides
Ascomycota |
Fungi
|
produced large amounts of 2-methyl-3-buten-2-ol (MB), the major component in the beetles’ aggregation pheromone blend, facilitating aggregation behavior |
Chemical biosynthesis
|
||
Sodalis praecaptivus
Pseudomonadota |
Bacteria
|
we investigated the role of a quorum sensing(QS ) system in S. praecaptivus and found that it negatively regulates a potent insect-killing phenotype |
- | ||
Fusarium euwallaceae
Ascomycota |
Fungi
|
Caring for the fungal gardens involves cooperative behavior, and could be related to the decrease of inter- and intra-specific competition for food |
Fungal farming
|
||
Raffaelea lauricola
Ascomycota |
Fungi
|
Caring for the fungal gardens involves cooperative behavior, and could be related to the decrease of inter- and intra-specific competition for food |
Fungal farming
|
||
Vairimorpha or a new genus
Microsporidia |
Fungi
|
Symptoms in infected adults were identified by an abnormal abdomen with malformation of the second pair of wings, impairing their flight activity. |
Growth and Development
|
||
Citrobacter freundii
Pseudomonadota |
Bacteria
|
affect the cellular and humoral immunity of the insect, increasing its susceptibility to Bacillus thuringiensis var. tenebrionis (morrisoni) (Bt) |
Immune priming
|
||
Penicillium herquei
Ascomycota |
Fungi
|
mycangial fungus may help alter leaf chemical components and protect against pathogens thus improve leaf-rolls for the development of E. chinesis |
Plant defense
Fungal farming
|
||
Wickerhamomyces anomalus
Ascomycota |
Fungi
|
fungal farming, a mutualistic nature of the D. bucculenta-W. anomalus association with morphological specialization and physiological dependence |
Fungal farming
|
||
Morganella morganii
Pseudomonadota |
Bacteria
|
Female beetles were previously shown to use phenol as their sex pheromone produced by symbiotic bacteria in the accessory or colleterial gland |
Chemical biosynthesis
|
||
Bacteria
|
are capable of producing a broad array of cellulases and hemicellulases, thus playing a major role in lignocellulosic biomass degradation |
Digestive enzymes
|
|||
Penicillium herquei
Ascomycota |
Fungi
|
P. herquei has the potential to synthesize or concentrate ergosterol, amino acids, and B vitamins and benefits the larvae of E. chinensis |
Nutrient provision
|
||
Citrobacter freundii
Pseudomonadota |
Bacteria
|
may produce 4,8-dimethyldecanal (DMD) production that is strongly associated with attraction to females and host pheromone communication |
Chemical biosynthesis
|
||
Escherichia coli
Pseudomonadota |
Bacteria
|
may produce 4,8-dimethyldecanal (DMD) production that is strongly associated with attraction to females and host pheromone communication |
Chemical biosynthesis
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
can be involved in the digestion of insect host’s food and plant secondary metabolites, which may increase the availability of nutrients |
Digestive enzymes
Plant secondary metabolites
Nutrient provision
|
||
Proteus vulgaris Ld01
Pseudomonadota |
Bacteria
|
produces toxic hydrogen cyanide (HCN) and a mandelonitrile-producing cyanoglucoside, amygdalin, which protect the insect from predation |
Natural enemy resistance
Chemical biosynthesis
|
||
Sodalis glossinidius
Pseudomonadota |
Bacteria
|
maintains and expresses inv/spa genes encoding a type III secretion system homologous to that used for invasion by bacterial pathogens |
- | ||
Fusarium solani
Ascomycota |
Fungi
|
weight and head capsule width were higher in larvae fed on F. solani, and gut lignocellulose activities were elevated in fed larvae |
Growth and Development
Digestive enzymes
|
||
Bacillus sp.
Bacillota |
Bacteria
|
The isolate has cellulolytic activity and can hydrolyze CMC, avicel, cellulose and sawdust with broad temperature and pH stability |
Digestive enzymes
|
||
Burkholderia
Pseudomonadota |
Bacteria
|
removal of the community significantly impairs the survival probability of young larvae when exposed to different pathogenic Fungi |
Antimicrobials
|
||
Streptomyces griseus XylebKG-1
Actinomycetota |
Bacteria
|
Cycloheximide is produced, which inhibits the growth of parasitic fungi Nectria spp. and protects mutualistic fungi Raffaelea spp. |
Antimicrobials
|
||
Bacillus flexus
Bacillota |
Bacteria
|
bacteria can degrade malathion, pirimiphos-methyl, and deltamethrin and utilize these insecticides as the carbon source in vitro. |
Pesticide metabolization
|
||
Bacillus licheniformis
Bacillota |
Bacteria
|
bacteria can degrade malathion, pirimiphos-methyl, and deltamethrin and utilize these insecticides as the carbon source in vitro. |
Pesticide metabolization
|
||
Bacillus subtilis
Bacillota |
Bacteria
|
bacteria can degrade malathion, pirimiphos-methyl, and deltamethrin and utilize these insecticides as the carbon source in vitro. |
Pesticide metabolization
|
||
Enterobacter sp.
Pseudomonadota |
Bacteria
|
bacteria can degrade malathion, pirimiphos-methyl, and deltamethrin and utilize these insecticides as the carbon source in vitro. |
Pesticide metabolization
|
||
Enterococcus faecalis
Bacillota |
Bacteria
|
bacteria can degrade malathion, pirimiphos-methyl, and deltamethrin and utilize these insecticides as the carbon source in vitro. |
Pesticide metabolization
|
||
Leptographium abietinum
Ascomycota |
Fungi
|
inoculation with L. abietinum significantly reduced concentrations of a tree defensive compound, (+)-4-carene, in growth media |
Plant secondary metabolites
|
||
Leptographium abietinum
Ascomycota |
Fungi
|
inoculation with L. abietinum significantly reduced concentrations of a tree defensive compound, (+)-3-carene, in growth media |
Plant secondary metabolites
|
||
Penicillium herquei
Ascomycota |
Fungi
|
associating with carbohydrate-active enzymes, cellulose and hemicellulose degradation, transporter, and terpenoid biosynthesis |
Digestive enzymes
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
toxins and polyketides have been implicated in the Pseudomonas-mediated protection of Paederus rove beetles against predators |
Natural enemy resistance
|
||
Citrobacter
Pseudomonadota |
Bacteria
|
can degrade plant polysaccharides and confer their host optimal adaptation to its environment by modulating its metabolism |
Sugar metabolism
|
||
Enterobacter
Pseudomonadota |
Bacteria
|
can degrade plant polysaccharides and confer their host optimal adaptation to its environment by modulating its metabolism |
Sugar metabolism
|
||
Klebsiella
Pseudomonadota |
Bacteria
|
can degrade plant polysaccharides and confer their host optimal adaptation to its environment by modulating its metabolism |
Sugar metabolism
|
||
Serratia
Pseudomonadota |
Bacteria
|
can degrade plant polysaccharides and confer their host optimal adaptation to its environment by modulating its metabolism |
Sugar metabolism
|
||
Symbiotaphrina kochii
Ascomycota |
Fungi
|
Antibiotic-treated insects suffered high mortality by phenoles. The symbiont showed phenol-degrading activities in vitro |
Plant secondary metabolites
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
Wolbachia directly favored weevil fertility and exhibited only mild indirect effects, usually enhancing the SZPE effect |
Fertility
|
||
Candida kashinagacola
Ascomycota |
Fungi
|
show extracelluar CM-cellulase, xylanase and avicelase activity that are responsible for degradation of wood structure |
Digestive enzymes
|
||
Meyerozyma guilliermondii
Ascomycota |
Fungi
|
show extracelluar CM-cellulase, xylanase and avicelase activity that are responsible for degradation of wood structure |
Digestive enzymes
|
||
Spiroplasma
Mycoplasmatota |
Bacteria
|
may manipulate host reproduction (e.g., cause male-killing) or provide resistance to nematodes and/or parasitoid wasps |
Reproductive manipulation
|
||
Staphylococcus gallinarum
Bacillota |
Bacteria
|
The strain encodes complete biosynthetic pathways for the production of B vitamins and amino acids, including tyrosine |
Nutrient provision
|
||
Enterococcus faecalis
Bacillota |
Bacteria
|
E. faecalis facilitate seed consumption by H. pensylvanicus, possibly by contributing digestive enzymes to their host |
Digestive enzymes
|
||
Grosmannia europhioides
Ascomycota |
Fungi
|
produced large amounts of 2-methyl-3-buten-2-ol (MB), the major component in the beetles' aggregation pheromone blend |
Chemical biosynthesis
|
||
Grosmannia penicillata
Ascomycota |
Fungi
|
produced large amounts of 2-methyl-3-buten-2-ol (MB), the major component in the beetles' aggregation pheromone blend |
Chemical biosynthesis
|
||
Acinetobacter
Pseudomonadota |
Bacteria
|
inhibited the expression of genes associated with the JA-mediated defense signaling pathway and SGA biosynthesis |
Plant defense
|
||
Citrobacter
Pseudomonadota |
Bacteria
|
inhibited the expression of genes associated with the JA-mediated defense signaling pathway and SGA biosynthesis |
Plant defense
|
||
Kodamaea ohmeri
Ascomycota |
Fungi
|
the volatiles produced by yeast-containing bee pollen dough eaten by beetle larvae are more attractive to adults |
- | ||
Grosmannia clavigera
Ascomycota |
Fungi
|
Increased success of host insect on jack pines (host plant) reduces food quality for interspecific competitors |
- | ||
Grosmannia clavigera
Ascomycota |
Fungi
|
fungal pathogenicity likely is more important in aiding MPB colonization and development within the host tree |
- | ||
Pseudomonas
Pseudomonadota |
Bacteria
|
could alleviate or compromise the antagonistic effects of fungi O. minus and L. procerum on RTB larval growth |
Growth and Development
Immune priming
|
||
Rahnella aquatilis
Pseudomonadota |
Bacteria
|
could alleviate or compromise the antagonistic effects of fungi O. minus and L. procerum on RTB larval growth |
Growth and Development
Immune priming
|
||
Serratia liquefaciens
Pseudomonadota |
Bacteria
|
could alleviate or compromise the antagonistic effects of fungi O. minus and L. procerum on RTB larval growth |
Growth and Development
Immune priming
|
||
Grosmannia clavigera
Ascomycota |
Fungi
|
Oxygenated monoterpenes produced by microbial activity is used as host (beetle) location cues by parasitoids |
- | ||
Penicillium herquei
Ascomycota |
Fungi
|
serve to inhibit microbial ‘weeds’ and pests, thus protecting the fungal garden against potential infection |
Fungal farming
Antimicrobials
|
||
Stammera
Pseudomonadota |
Bacteria
|
produce symbiont-derived pectinases and supply to the host’s alimentary tract for plant cell wall digestion |
Digestive enzymes
|
||
Acinetobacter sp. AS23
Pseudomonadota |
Bacteria
|
facilitate the degradation of tea saponin; genome contains 47 genes relating to triterpenoids degradation |
Plant secondary metabolites
|
||
Streptomyces
Actinomycetota |
Bacteria
|
resulting in a rich repertoire of antimicrobials, inhibit a fungal entomopathogen, Metarhizium anisopliae |
Antimicrobials
|
||
Candidatus Dasytiphilus stammeri Daer
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Dalp
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Dlin
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri DngrGER
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri DngrITA
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Dplu
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Dsem
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Dvir
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Lsp00
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Lsp01
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Lsp02
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Lsp04
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Lsp06
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Lsp07
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Lsp09
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Candidatus Dasytiphilus stammeri Pvir
Pseudomonadota |
Bacteria
|
contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. |
Nutrient provision
|
||
Rahnella aquatilis
Pseudomonadota |
Bacteria
|
R. aquatilis decreased (−)-α-pinene (38%) and (+)-α-pinene (46%) by 40% and 45% (by GC-MS), respectively |
Plant secondary metabolites
|
||
Serratia marcescens 2MH3-2
Pseudomonadota |
Bacteria
|
producing antibacterial compound Serrawettin W2, which has antibacterial and nematode-inhibiting effects |
Antimicrobials
|
||
Ambrosiella grosmanniae
Ascomycota |
Fungi
|
X. germanus exhibited an arrestment response to volatiles of A. grosmanniae, but not antagonistic fungi |
- | ||
Bacteroides
Bacteroidota |
Bacteria
|
supplement precursors for the cuticle synthesis and thereby enhance desiccation resistance of its host |
- | ||
Enterobacter spp.
Pseudomonadota |
Bacteria
|
Bacteria isolated from pine engravers decreased concentrations of (-)-α-pinene, myrcene, and 3-carene |
- | ||
Erwinia spp.
Pseudomonadota |
Bacteria
|
Bacteria isolated from pine engravers decreased concentrations of (-)-α-pinene, myrcene, and 3-carene |
- | ||
Serratia spp.
Pseudomonadota |
Bacteria
|
Bacteria isolated from pine engravers decreased concentrations of (-)-α-pinene, myrcene, and 3-carene |
- | ||
Sodalis pierantonius
Pseudomonadota |
Bacteria
|
produce vitamins and essential amino acids required for insect development and cuticle biosynthesis |
Nutrient provision
|
||
Enterobacter cloacae
Pseudomonadota |
Bacteria
|
promote the development and body mass gain of RPW larvae by improving their nutrition metabolism |
Nutrient provision
Growth and Development
|
||
Lactococcus lactis
Bacillota |
Bacteria
|
promote the development and body mass gain of RPW larvae by improving their nutrition metabolism |
Nutrient provision
Growth and Development
|
||
Bacteria and Fungi
|
to preserve carrion quality and support larval growth in a challenging resource such as carrion. |
- | |||
Acinetobacter lwoffi
Pseudomonadota |
Bacteria
|
extreme cellulolytic enzymes, at extreme (pH 14) conditions, exhibited cellulolytic properties |
Digestive enzymes
|
||
Microbacterium paraoxydan
Actinomycetota |
Bacteria
|
extreme cellulolytic enzymes, at extreme (pH 13) conditions, exhibited cellulolytic properties |
Digestive enzymes
|
||
Micrococcus sp.
Actinomycetota |
Bacteria
|
extreme cellulolytic enzymes, at extreme (pH 12) conditions, exhibited cellulolytic properties |
Digestive enzymes
|
||
Stammera
Pseudomonadota |
Bacteria
|
decoupled in adult beetles to match the nutritional and reproductive requirements of its host. |
Fertility
Nutrient provision
|
||
Citrobacter
Pseudomonadota |
Bacteria
|
associated with nitrogen fixation, recycling of uric acid nitrogen, and cellulose degradation |
Nitrogen fixation
Digestive enzymes
|
||
Citrobacter
Pseudomonadota |
Bacteria
|
associated with nitrogen fixation, recycling of uric acid nitrogen, and cellulose degradation |
Nitrogen fixation
Digestive enzymes
|
||
Paludibacter propionicigenes
Bacteroidota |
Bacteria
|
microbial fixation of nitrogen that is important for this beetle to subsist on woody biomass |
Nitrogen fixation
|
||
Candidatus Sodalis pierantonius
Pseudomonadota |
Bacteria
|
Tyrosine precursor provisioning, supplementation of some essential amino acids and vitamins |
Nutrient provision
|
||
Sodalis pierantonius
Pseudomonadota |
Bacteria
|
may infulence immunity, metabolism, metal control, apoptosis, and bacterial stress response |
Immune priming
|
||
Candidatus Sodalis pierantonius str. SZPE
Pseudomonadota |
Bacteria
|
SZPE suppression delayed weevil emergence, which reduced the insect population growth rate |
Growth and Development
|
||
Corynebacterium variabile
Actinomycetota |
Bacteria
|
terpenoid-degrading: the highest degradation rates of D-camphor, linalool, and eucalyptol |
Plant secondary metabolites
|
||
Morganella morganii
Pseudomonadota |
Bacteria
|
symbionts residing in the colleterial glands produce phenol 1 as the female sex pheromone |
Chemical biosynthesis
|
||
Pseudomonas aeruginosa
Pseudomonadota |
Bacteria
|
terpenoid-degrading: the highest degradation rates of D-camphor, linalool, and eucalyptol |
Plant secondary metabolites
|
||
Serratia marcescens
Pseudomonadota |
Bacteria
|
terpenoid-degrading: the highest degradation rates of D-camphor, linalool, and eucalyptol |
Plant secondary metabolites
|
||
Beauveria bassiana
Ascomycota |
Fungi
|
B. bassiana has the insecticidal activity on X. affinis adult females and their progeny |
Fertility
|
||
Morganella morganii
Pseudomonadota |
Bacteria
|
produces phenol as the sex pheromone of the host from tyrosine in the colleterial gland |
Chemical biosynthesis
|
||
Acremonium
Ascomycota |
Fungi
|
may grow confined mostly in beetle galleries and play a role in the beetle's nutrition |
Nutrient provision
|
||
Acremonium masseei
Ascomycota |
Fungi
|
may grow confined mostly in beetle galleries and play a role in the beetle's nutrition |
Nutrient provision
|
||
Acremonium morum
Ascomycota |
Fungi
|
may grow confined mostly in beetle galleries and play a role in the beetle's nutrition |
Nutrient provision
|
||
Rahnella sp. ChDrAdgB13
Pseudomonadota |
Bacteria
|
has metabolic capacity to degrade xylan by bifunctional xylanase-ferulic acid esterase |
Digestive enzymes
|
||
Endoconidiophora rufipennis
Ascomycota |
Fungi
|
Semiochemicals produced by symbiont can act as an anti-attractant for Ips typographus |
Chemical biosynthesis
|
||
Rickettsia
Pseudomonadota |
Bacteria
|
inducing cytoplasmic incompatibility, resulting in reproductive distortions and hence |
Reproductive manipulation
|
||
Scheffersomyces insectosa
Ascomycota |
Fungi
|
assimilated wood-associated sugars including xylose, cellobiose, and xylan in culture |
Digestive enzymes
|
||
Serratia proteamaculans
Pseudomonadota |
Bacteria
|
display strong cellulolytic activity and process a single endoglucanase encoding gene |
Digestive enzymes
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
inducing cytoplasmic incompatibility, resulting in reproductive distortions and hence |
Reproductive manipulation
|
||
Nardonella
Pseudomonadota |
Bacteria
|
tyrosine provisioning, which is needed for insect’s cuticle formation and hardening |
Nutrient provision
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
It is primarily responsible for suppression of plant defenses in tomato and potato. |
Plant defense
|
||
Pseudomonas sp
Pseudomonadota |
Bacteria
|
Pseudomonas sp. core bacteria can promote host infection by entomopathogenic fungus |
- | ||
Pantoea
Pseudomonadota |
Bacteria
|
participate in the degradation, utilization of different types of plant materials |
Digestive enzymes
|
||
Pseudomonas aeruginosa
Pseudomonadota |
Bacteria
|
degrade low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE) |
Plastic degradation
|
||
Rickettsia
Pseudomonadota |
Bacteria
|
may be associated with insect reproduction and maturation of their sexual organs |
Fertility
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
may be associated with insect reproduction and maturation of their sexual organs |
Fertility
|
||
Wolbachia strain wSur
Pseudomonadota |
Bacteria
|
causing cytoplasmic incompatibility but not male-killing in a grain pest beetle |
Reproductive manipulation
|
||
Streptomyces sp. AT67
Actinomycetota |
Bacteria
|
contribute brood ball hygiene by inhibiting fungal parasites in the environment |
Antimicrobials
|
||
Bradyrhizobium
Pseudomonadota |
Bacteria
|
be commonly found in plant roots and they all have nitrogen fixation abilities |
Plant defense
|
||
Burkholderia
Pseudomonadota |
Bacteria
|
Genera contained most genes involved in terpene degradation (by metagenomics) |
Plant secondary metabolites
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
Genera contained most genes involved in terpene degradation (by metagenomics) |
Plant secondary metabolites
|
||
Pseudomonas typographi
Pseudomonadota |
Bacteria
|
P. typographi aids I. typographi nutrition and resistance to fungal pathogens |
Antimicrobials
Nutrient provision
|
||
Rahnella
Pseudomonadota |
Bacteria
|
Genera contained most genes involved in terpene degradation (by metagenomics) |
Plant secondary metabolites
|
||
Rickettsia
Pseudomonadota |
Bacteria
|
potential defensive properties against he parasitoid Microctonus aethiopoides |
Natural enemy resistance
|
||
Serratia
Pseudomonadota |
Bacteria
|
Genera contained most genes involved in terpene degradation (by metagenomics) |
Plant secondary metabolites
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
potential defensive properties against he parasitoid Microctonus aethiopoides |
Natural enemy resistance
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
infecting A. fraudatrix causes cytoplasmic incompatibility in the host insect |
- | ||
Nardonella spp.
Pseudomonadota |
Bacteria
|
endosymbiont is involved in normal growth and development of the host weevil |
Growth and Development
|
||
Klebsiella oxytoca
Pseudomonadota |
Bacteria
|
plastic-degrading properties against bioplastics such as PBSA, PBS and PCL. |
Plastic degradation
|
||
Ophiostoma minus
Ascomycota |
Fungi
|
The phenoloxidase ratio increased significantly in the larvae with O. minus |
Immune priming
|
||
Pseudomonas aeruginosa
Pseudomonadota |
Bacteria
|
plastic-degrading properties against bioplastics such as PBSA, PBS and PCL. |
Plastic degradation
|
||
Serratia marcescens
Pseudomonadota |
Bacteria
|
plastic-degrading properties against bioplastics such as PBSA, PBS and PCL. |
Plastic degradation
|
||
Fusarium ambrosium
Ascomycota |
Fungi
|
associated with adult beetles and lesions surrounding the beetle galleries |
- | ||
Fusarium ambrosium
Ascomycota |
Fungi
|
associated with adult beetles and lesions surrounding the beetle galleries |
- | ||
Wolbachia
Pseudomonadota |
Bacteria
|
Wolbachia are necessary for oocyte production in Lissorhoptrus oryzophilus |
Reproductive manipulation
|
||
Nardonella
Pseudomonadota |
Bacteria
|
might be not playing critical roles in the reproduction of L. oryzophilus |
- | ||
Ophiostoma ips
Ascomycota |
Fungi
|
suppress decomposition of pine sapwood by competing with wood-decay fungi |
Plant defense
|
||
Ophiostoma ips
Ascomycota |
Fungi
|
suppress decomposition of pine sapwood by competing with wood-decay fungi |
Plant defense
|
||
Ophiostoma ips
Ascomycota |
Fungi
|
suppress decomposition of pine sapwood by competing with wood-decay fungi |
Plant defense
|
||
Raffaelea fusca
Ascomycota |
Fungi
|
suppress decomposition of pine sapwood by competing with wood-decay fungi |
Plant defense
|
||
Raffaelea fusca
Ascomycota |
Fungi
|
suppress decomposition of pine sapwood by competing with wood-decay fungi |
Plant defense
|
||
Raffaelea fusca
Ascomycota |
Fungi
|
suppress decomposition of pine sapwood by competing with wood-decay fungi |
Plant defense
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
mediate the down-regulation of many maize defenses via their insect hosts |
Plant defense
|
||
Acremonium sp.
Ascomycota |
Fungi
|
fungal volatiles as attractive cues during host selection by X. germanus |
- | ||
Enterobacter
Pseudomonadota |
Bacteria
|
It is primarily responsible for suppression of plant defenses in potato. |
Plant defense
|
||
Enterococcus faecalis
Bacillota |
Bacteria
|
modulates host phosphine resistance by interfering with the redox system |
- | ||
Stenotrophomonas
Pseudomonadota |
Bacteria
|
It is primarily responsible for suppression of plant defenses in tomato. |
Plant defense
|
||
Wickerhamomyces anomalus
Ascomycota |
Fungi
|
fungal garden making inside bamboos by non-social fungus-farming insects |
Fungal farming
|
||
Acinetobacter sp.
Pseudomonadota |
Bacteria
|
might contribute to caffeine breakdown using the C-11 oxidation pathway |
Plant secondary metabolites
|
||
Delftia sp.
Pseudomonadota |
Bacteria
|
might contribute to caffeine breakdown using the C-19 oxidation pathway |
Plant secondary metabolites
|
||
Enterococcus sp.
Bacillota |
Bacteria
|
might contribute to caffeine breakdown using the C-10 oxidation pathway |
Plant secondary metabolites
|
||
Erwinia sp.
Pseudomonadota |
Bacteria
|
might contribute to caffeine breakdown using the C-12 oxidation pathway |
Plant secondary metabolites
|
||
Klebsiella sp.
Pseudomonadota |
Bacteria
|
might contribute to caffeine breakdown using the C-17 oxidation pathway |
Plant secondary metabolites
|
||
Kosakonia sp.
Pseudomonadota |
Bacteria
|
might contribute to caffeine breakdown using the C-16 oxidation pathway |
Plant secondary metabolites
|
||
Lactococcus sp.
Bacillota |
Bacteria
|
might contribute to caffeine breakdown using the C-13 oxidation pathway |
Plant secondary metabolites
|
||
Leuconostoc sp.
Bacillota |
Bacteria
|
might contribute to caffeine breakdown using the C-18 oxidation pathway |
Plant secondary metabolites
|
||
Pantoea sp.
Pseudomonadota |
Bacteria
|
might contribute to caffeine breakdown using the C-14 oxidation pathway |
Plant secondary metabolites
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
having a role in insect egg protection against attack by other microbes |
Antimicrobials
|
||
Pseudomonas sp.
Pseudomonadota |
Bacteria
|
might contribute to caffeine breakdown using the C-15 oxidation pathway |
Plant secondary metabolites
|
||
Stenotrophomonas sp.
Pseudomonadota |
Bacteria
|
might contribute to caffeine breakdown using the C-20 oxidation pathway |
Plant secondary metabolites
|
||
Acinetobacter sp. AnTc-1
Pseudomonadota |
Bacteria
|
may play a role in the larval gut for biodegradation of Polystyrene PS |
Plastic degradation
|
||
Bacillus sp.
Bacillota |
Bacteria
|
might contribute to caffeine breakdown using the C-8 oxidation pathway |
Plant secondary metabolites
|
||
Enterococcus
Bacillota |
Bacteria
|
implicated in the production of fecal aggregation pheromone components |
Chemical biosynthesis
|
||
Paenibacillus sp.
Bacillota |
Bacteria
|
might contribute to caffeine breakdown using the C-9 oxidation pathway |
Plant secondary metabolites
|
||
Cyberlindnera americana ChDrAdgY46
Ascomycota |
Fungi
|
play a role in the detoxification process of tree defensive chemicals |
Plant secondary metabolites
|
||
Bacteria
|
digestive symbiosis with potential plant cell wall degrading microbes |
Digestive enzymes
|
|||
Bacteria
|
beetle-associated bacterial symbionts mediate tea saponin degradation |
Digestive enzymes
Plant secondary metabolites
|
|||
Bacteria
|
digestive symbiosis with potential plant cell wall degrading microbes |
Digestive enzymes
|
|||
Leptographium procerum
Ascomycota |
Fungi
|
Inducing host pines to produce 3-carene, an attractant of the beetle |
Chemical biosynthesis
|
||
Aspergillus sp.
Ascomycota |
Fungi
|
decreased the levels of soluble carbohydrate, cellulose, and lignin |
Digestive enzymes
|
||
Cladosporium sp.
Ascomycota |
Fungi
|
decreased the levels of soluble carbohydrate, cellulose, and lignin |
Digestive enzymes
|
||
Penicillium sp.
Ascomycota |
Fungi
|
decreased the levels of soluble carbohydrate, cellulose, and lignin |
Digestive enzymes
|
||
Candidatus Mesenet longicola
Pseudomonadota |
Bacteria
|
induced complete Cytoplasmic incompatibility (CI) (100% mortality) |
Reproductive manipulation
|
||
Halomonas
Pseudomonadota |
Bacteria
|
Have the ability for degradation of cellulose, proteins and starch |
Digestive enzymes
|
||
Pseudomonas mandelii
Pseudomonadota |
Bacteria
|
P. mandelii decreased concentrations of all monoterpenes by 15–24% |
Plant secondary metabolites
|
||
Serratia marcescens
Pseudomonadota |
Bacteria
|
produces an antibacterial cyclic lipopeptide called serrawettin W2 |
Antimicrobials
|
||
Vibrio
Pseudomonadota |
Bacteria
|
Have the ability for degradation of cellulose, proteins and starch |
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
Amino acid and B vitamin supplementation, plant biomass digestion |
Nutrient provision
Digestive enzymes
|
||
Bacteria
|
Defense against pathogenic bacteria (via host immune stimulation) |
Pathogen interaction
|
|||
wBruAus
Pseudomonadota |
Bacteria
|
wBruAus is exceptionally resistant to tetracycline and rifampicin |
Pesticide metabolization
|
||
Wolbachia sp.
Pseudomonadota |
Bacteria
|
Silencing of maize (host plant) defence induction via insect host |
Plant defense
|
||
Streptomyces
Actinomycetota |
Bacteria
|
Defense against antagonistic fungus of the beetle's cultivar |
Antimicrobials
|
||
Enterobacter
Pseudomonadota |
Bacteria
|
Anti-phytopathogenic fungi activity; growth and development |
Antimicrobials
|
||
Citrobacter
Pseudomonadota |
Bacteria
|
provide nitrogen fixation to hosts for desert environments |
Nitrogen fixation
|
||
Enterobacter
Pseudomonadota |
Bacteria
|
provide nitrogen fixation to hosts for desert environments |
Nitrogen fixation
|
||
Klebsiella pneumonia
Pseudomonadota |
Bacteria
|
provide nitrogen fixation to hosts for desert environments |
Nitrogen fixation
|
||
Klebsiella spp.
Pseudomonadota |
Bacteria
|
provide nitrogen fixation to hosts for desert environments |
Nitrogen fixation
|
||
Klebsiella spp.
Pseudomonadota |
Bacteria
|
provide nitrogen fixation to hosts for desert environments |
Nitrogen fixation
|
||
Raffaelea lauricola
Ascomycota |
Fungi
|
Host tree pathogen and nutrition provision during invasion |
Nutrient provision
Antimicrobials
|
||
Pseudomonas chlororaphis
Pseudomonadota |
Bacteria
|
Against Bacterial Symbionts of Entomopathogenic Nematodes |
Natural enemy resistance
|
||
Serritia marcescens
Pseudomonadota |
Bacteria
|
S. marcescens reduced 49–79% of 3-carene and (−)-β-pinene |
Plant secondary metabolites
|
||
Fusarium solani
Ascomycota |
Fungi
|
promoters of the pathogenic behavior of ambrosia beetles |
- | ||
Bacteria
|
confer protection by priming the immune system of host |
Immune priming
|
|||
Burkholderia
Pseudomonadota |
Bacteria
|
provisioning of essential amino acids and/or vitamins |
Nutrient provision
|
||
Burkholderia
Pseudomonadota |
Bacteria
|
provisioning of essential amino acids and/or vitamins |
Nutrient provision
|
||
Pantoea
Pseudomonadota |
Bacteria
|
contribute to detoxification of toxic isothiocyanates |
Pesticide metabolization
|
||
wBruCon
Pseudomonadota |
Bacteria
|
caused cytoplasmic incompatibility of the host insect |
Reproductive manipulation
|
||
wBruOri
Pseudomonadota |
Bacteria
|
caused cytoplasmic incompatibility of the host insect |
Reproductive manipulation
|
||
Enterobacter
Pseudomonadota |
Bacteria
|
may help M. alternatus degrade cellulose and pinene |
Digestive enzymes
Plant secondary metabolites
|
||
Grosmannia europhioides
Ascomycota |
Fungi
|
fungi have the ability to degrade conifer phenolics |
Plant secondary metabolites
|
||
Grosmannia penicillata
Ascomycota |
Fungi
|
fungi have the ability to degrade conifer phenolics |
Plant secondary metabolites
|
||
Bacteria
|
degrade both natural and synthetic plastic polymers |
Plastic degradation
|
|||
Lactococcus
Bacillota |
Bacteria
|
may help M. alternatus degrade cellulose and pinene |
Digestive enzymes
Plant secondary metabolites
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
may help M. alternatus degrade cellulose and pinene |
Digestive enzymes
Plant secondary metabolites
|
||
Raoultella
Pseudomonadota |
Bacteria
|
may help M. alternatus degrade cellulose and pinene |
Digestive enzymes
Plant secondary metabolites
|
||
Serratia
Pseudomonadota |
Bacteria
|
may help M. alternatus degrade cellulose and pinene |
Digestive enzymes
Plant secondary metabolites
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
influence down-regulation of defense genes in maize |
Plant defense
|
||
Acinetobacter sp. AS23
Pseudomonadota |
Bacteria
|
endow its host with the ability to degrade saponin |
Plant secondary metabolites
|
||
Candidatus Curculioniphilus buchneri
Pseudomonadota |
Bacteria
|
represent the primary symbiont of Curculio weevils |
- | ||
Candidatus Curculioniphilus buchneri
Pseudomonadota |
Bacteria
|
represent the primary symbiont of Curculio weevils |
- | ||
Candidatus Curculioniphilus buchneri
Pseudomonadota |
Bacteria
|
represent the primary symbiont of Curculio weevils |
- | ||
Candidatus Curculioniphilus buchneri
Pseudomonadota |
Bacteria
|
represent the primary symbiont of Curculio weevils |
- | ||
Stenotrophomonas maltophilia
Pseudomonadota |
Bacteria
|
correlated with polyvinyl chloride PVC degradation |
Plastic degradation
|
||
Ambrosiozyma sp.
Ascomycota |
Fungi
|
show CM-cellulase activity and pectinase activity |
Digestive enzymes
|
||
Candida homilentoma
Ascomycota |
Fungi
|
show CM-cellulase activity and pectinase activity |
Digestive enzymes
|
||
Cronobacter
Pseudomonadota |
Bacteria
|
may be indirectly involved in the digestion of PE |
Plastic degradation
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
degrade additive-free polypropylene (PP) plastics |
Plastic degradation
|
||
Bacillus cereus ATCC 14579
Bacillota |
Bacteria
|
provide symbiotic digestive functions to Oryctes |
Digestive enzymes
|
||
Bacteria
|
gut microbes contribute to nitrogen provisioning |
Nutrient provision
Nitrogen fixation
|
|||
Bacillus cereus
Bacillota |
Bacteria
|
might be promising paratransgenesis candidates |
- | ||
Cryptococcus sp.
Basidiomycota |
Fungi
|
has the potential of degrading plant cell wall |
Digestive enzymes
|
||
Enterobacter sp.
Pseudomonadota |
Bacteria
|
might be promising paratransgenesis candidates |
- | ||
Enterococcus faecalis
Bacillota |
Bacteria
|
might be promising paratransgenesis candidates |
- | ||
Kuraishia molischiana
Ascomycota |
Fungi
|
has the potential of degrading plant cell wall |
Digestive enzymes
|
||
Nakazawaea ambrosiae
Ascomycota |
Fungi
|
has the potential of degrading plant cell wall |
Digestive enzymes
|
||
Ogataea ramenticola
Ascomycota |
Fungi
|
has the potential of degrading plant cell wall |
Digestive enzymes
|
||
Wickerhamomyces bisporus
Ascomycota |
Fungi
|
has the potential of degrading plant cell wall |
Digestive enzymes
|
||
Pantoea
Pseudomonadota |
Bacteria
|
might play a role in detoxifying cycad toxins |
Plant secondary metabolites
|
||
Pantoea
Pseudomonadota |
Bacteria
|
might play a role in detoxifying cycad toxins |
Plant secondary metabolites
|
||
Rickettsia
Pseudomonadota |
Bacteria
|
kill male host offspring during embryogenesis |
Reproductive manipulation
|
||
Serratia
Pseudomonadota |
Bacteria
|
might play a role in detoxifying cycad toxins |
Plant secondary metabolites
|
||
Serratia
Pseudomonadota |
Bacteria
|
might play a role in detoxifying cycad toxins |
Plant secondary metabolites
|
||
Stenotrophomonas
Pseudomonadota |
Bacteria
|
might play a role in detoxifying cycad toxins |
Plant secondary metabolites
|
||
Stenotrophomonas
Pseudomonadota |
Bacteria
|
might play a role in detoxifying cycad toxins |
Plant secondary metabolites
|
||
Enterobacteriaceae
Pseudomonadota |
Bacteria
|
degrade the diterpene acids of Norway spruce |
Plant secondary metabolites
|
||
Paludibacter propionicigenes
Bacteroidota |
Bacteria
|
plays an important role in nitrogen fixation |
Nitrogen fixation
|
||
Enterobacteriaceae
Pseudomonadota |
Bacteria
|
produce cellulases under certain conditions |
Digestive enzymes
|
||
Bacteria
|
Detoxification of plant secondary compounds |
Plant secondary metabolites
|
|||
Bacteria
|
Detoxification of plant secondary compounds |
Plant secondary metabolites
|
|||
Klebsiella
Pseudomonadota |
Bacteria
|
ability to fix nitrogen from the atmosphere |
Nitrogen fixation
|
||
Pantoea
Pseudomonadota |
Bacteria
|
Detoxification of plant secondary compounds |
Plant secondary metabolites
|
||
Pseudomonas fulva
Pseudomonadota |
Bacteria
|
Detoxification of plant secondary compounds |
Plant secondary metabolites
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
it causes nucleocytoplasmic incompatibility |
Reproductive manipulation
|
||
Rahnella
Pseudomonadota |
Bacteria
|
It may specialize in terpenoid metabolism. |
Plant secondary metabolites
|
||
Serratia
Pseudomonadota |
Bacteria
|
It may specialize in terpenoid metabolism. |
Plant secondary metabolites
|
||
Leptographium procerum
Ascomycota |
Fungi
|
compete with RTB larvae for carbohydrates |
- | ||
Ophiostoma minus
Ascomycota |
Fungi
|
compete with RTB larvae for carbohydrates |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
required for oogenesis in C. dactyliperda |
Fertility
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
required for oogenesis in C. dactyliperda |
Fertility
|
||
Candidatus Nardonella
Pseudomonadota |
Bacteria
|
Possibly tyrosine precursor provisioning |
Nutrient provision
|
||
Candidatus Shikimatogenerans
Bacteroidota |
Bacteria
|
Possibly tyrosine precursor provisioning |
Nutrient provision
|
||
Candidatus Shikimatogenerans
Bacteroidota |
Bacteria
|
Possibly tyrosine precursor provisioning |
Nutrient provision
|
||
Citrobacter koseri LMG 5519
Pseudomonadota |
Bacteria
|
associated with insect digestive tracts |
Digestive enzymes
|
||
Pseudomonas sp,
Pseudomonadota |
Bacteria
|
Degraded 20–50% of α-pinene (by GC-MS) |
Plant secondary metabolites
|
||
Rahnella aquatilis
Pseudomonadota |
Bacteria
|
Degraded 20–50% of α-pinene (by GC-MS) |
Plant secondary metabolites
|
||
Serratia sp.
Pseudomonadota |
Bacteria
|
Degraded 20–50% of α-pinene (by GC-MS) |
Plant secondary metabolites
|
||
Grosmannia penicillata
Ascomycota |
Fungi
|
produce beetle aggregation pheromones |
Chemical biosynthesis
|
||
Klebsiella
Pseudomonadota |
Bacteria
|
degrade polybutylene succinate (PBS) |
Plastic degradation
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
kill male hosts during embryogenesis |
Reproductive manipulation
|
||
Wolbachia pipientis
Pseudomonadota |
Bacteria
|
induces cytoplasmic incompatibility |
Reproductive manipulation
|
||
Wolbachia pipientis
Pseudomonadota |
Bacteria
|
induces cytoplasmic incompatibility |
Reproductive manipulation
|
||
Candida xylanilytica KU-Xn11T
Ascomycota |
Fungi
|
extracellular cellulase production |
Digestive enzymes
|
||
Nardonella
Pseudomonadota |
Bacteria
|
participate in tyrosine production |
Nutrient provision
|
||
Yarrowia yeasts
Ascomycota |
Fungi
|
Defense against competing microbes |
Antimicrobials
|
||
Cladosporium
Ascomycota |
Fungi
|
Produce many antimicrobial agents |
Antimicrobials
|
||
Enterococcus
Bacillota |
Bacteria
|
associated with PE biodegradation |
Plastic degradation
|
||
Bacteria
|
Bamboo lignocellulose degradation |
Digestive enzymes
|
|||
Lactococcus
Bacillota |
Bacteria
|
associated with PE biodegradation |
Plastic degradation
|
||
Spiroplasma
Mycoplasmatota |
Bacteria
|
associated with PE biodegradation |
Plastic degradation
|
||
Trabulsiella
Pseudomonadota |
Bacteria
|
Involved in cellulose degradation |
Digestive enzymes
|
||
Citrobacter koseri
Pseudomonadota |
Bacteria
|
degrade polyvinyl chloride (PVC) |
Plastic degradation
|
||
Mycobacterium
Actinomycetota |
Bacteria
|
produces Antimicrobial compounds |
Antimicrobials
|
||
Candidatus Nardonella
Pseudomonadota |
Bacteria
|
Tyrosine precursor provisioning |
Nutrient provision
|
||
Candidatus Nardonella
Pseudomonadota |
Bacteria
|
Tyrosine precursor provisioning |
Nutrient provision
|
||
Candidatus Nardonella
Pseudomonadota |
Bacteria
|
Tyrosine precursor provisioning |
Nutrient provision
|
||
Candidatus Nardonella
Pseudomonadota |
Bacteria
|
Tyrosine precursor provisioning |
Nutrient provision
|
||
Dysgonomonas sp.
Bacteroidota |
Bacteria
|
associated with PET degradation |
Plastic degradation
|
||
Hafnia-Obesumbacterium sp.
Pseudomonadota |
Bacteria
|
associated with PET degradation |
Plastic degradation
|
||
Spiroplasma sp.
Mycoplasmatota |
Bacteria
|
associated with PET degradation |
Plastic degradation
|
||
Burkholderia
Pseudomonadota |
Bacteria
|
Involved in nitrogen recycling |
Nitrogen fixation
|
||
Wolbachia
Pseudomonadota |
Bacteria
|
induces embryonic male killing |
Reproductive manipulation
|
||
Bacteria
|
degrading ellulose and xylan |
Digestive enzymes
|
|||
Lactococcus
Bacillota |
Bacteria
|
degrading ellulose and xylan |
Digestive enzymes
|
||
Turicibacter
Bacillota |
Bacteria
|
degrading ellulose and xylan |
Digestive enzymes
|
||
Enterococcus faecalis
Bacillota |
Bacteria
|
contribute to seed digestion |
Digestive enzymes
|
||
Bacteria
|
Inhibition of plant defenses |
Plant defense
|
|||
Achromobacter xylosoxidans M9
Pseudomonadota |
Bacteria
|
degrade polyethylene(PE) |
Plastic degradation
|
||
Burkholderia gladioli
Pseudomonadota |
Bacteria
|
Egg antifungal protection |
Antimicrobials
|
||
Burkholderia gladioli
Pseudomonadota |
Bacteria
|
Defense against pathogens |
Pathogen interaction
|
||
Enterobacter
Pseudomonadota |
Bacteria
|
suppressed plant defenses |
Plant defense
|
||
Enterobacter hormaechei LG3
Pseudomonadota |
Bacteria
|
degrade polyethylene (PE) |
Plastic degradation
|
||
Pantoea
Pseudomonadota |
Bacteria
|
suppressed plant defenses |
Plant defense
|
||
Pseudomonas aeruginosa M2
Pseudomonadota |
Bacteria
|
degrade polyethylene(PE) |
Plastic degradation
|
||
Pseudomonas aeruginosa M8
Pseudomonadota |
Bacteria
|
degrade polyethylene(PE) |
Plastic degradation
|
||
Pseudomonas M7
Pseudomonadota |
Bacteria
|
degrade polyethylene(PE) |
Plastic degradation
|
||
Pseudomonas spp.
Pseudomonadota |
Bacteria
|
Defense against predators |
Natural enemy resistance
|
||
Pseudomonas stutzeri M3
Pseudomonadota |
Bacteria
|
degrade polyethylene(PE) |
Plastic degradation
|
||
Acinetobacter sp. BIT-H3
Pseudomonadota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Cellulosimicrobium sp. WJ2025
Actinomycetota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Citrobacter
Pseudomonadota |
Bacteria
|
degrading lignocellulose |
Digestive enzymes
|
||
Citrobacter sp.
Pseudomonadota |
Bacteria
|
degrade polystyrene (PS) |
Plastic degradation
|
||
Klebsiella aerogenes strain DAI2m/a
Pseudomonadota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Klebsiella sp. WJ2020
Pseudomonadota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Kosakonia sp.
Pseudomonadota |
Bacteria
|
degrade polystyrene (PS) |
Plastic degradation
|
||
Mixta tenebrionis BIT-26
Pseudomonadota |
Bacteria
|
degrade polystyrene (PS) |
Plastic degradation
|
||
Pseudomonas aeruginosa strain DAI2m/b
Pseudomonadota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Pseudomonas aeruginosa strain DSM 50071
Pseudomonadota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Pseudomonas putida H-01
Pseudomonadota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Serratia sp.
Pseudomonadota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Stenotrophomonas maltophilia strain DAI2m/c
Pseudomonadota |
Bacteria
|
degrade Polystyrene (PS) |
Plastic degradation
|
||
Candidatus Stammera capleta
Pseudomonadota |
Bacteria
|
Plant biomass digestion |
Digestive enzymes
|
||
Bacteria
|
degrade Lignocellulose |
Digestive enzymes
|
|||
Burkholderia gladioli Lv-StA
Pseudomonadota |
Bacteria
|
Antibiotic production |
Antimicrobials
|
||
Aeromonas sp. TM1
Pseudomonadota |
Bacteria
|
degrading plastics |
Plastic degradation
|
||
Aeromonas sp. TM1
Pseudomonadota |
Bacteria
|
degrading plastics |
Plastic degradation
|
||
Citrobacter
Pseudomonadota |
Bacteria
|
degrading plastics |
Plastic degradation
|
||
Exiguobacterium sp. YT2
Bacillota |
Bacteria
|
degrading plastics |
Plastic degradation
|
||
Klebsiella pneumoniae ZM1
Pseudomonadota |
Bacteria
|
degrading plastics |
Plastic degradation
|
||
Klebsiella pneumoniae ZM1
Pseudomonadota |
Bacteria
|
degrading plastics |
Plastic degradation
|
||
Kosakonia
Pseudomonadota |
Bacteria
|
degrading plastics |
Plastic degradation
|
||
Rhodococcus ruber
Actinomycetota |
Bacteria
|
degrading plastics |
Plastic degradation
|
||
Bacteria
|
Nitrogen fixation |
Nitrogen fixation
|
|||
Scheffersomyces insectosa
Ascomycota |
Fungi
|
xylose-fermenting |
Sugar metabolism
|
||
Cylindrobasidium ipidophilum
Basidiomycota |
Fungi
|
wood decay fungi |
- | ||
Spiroplasma
Mycoplasmatota |
Bacteria
|
male killing |
Reproductive manipulation
|
||
Bacteria
|
gut microbe |
- | |||
Bacillus toyonensis BCT-7112
Bacillota |
Bacteria
|
gut microbe |
- | ||
Candida tropicalis ATCC 75None
Ascomycota |
Fungi
|
gut microbe |
- | ||
Comamonas nitrativorans 2331None
Pseudomonadota |
Bacteria
|
gut microbe |
- | ||
Diaphorobacter aerolatus 86None4S-37 like
Pseudomonadota |
Bacteria
|
gut microbe |
- | ||
Klebsiella pneuomoniae DSM 3None1None4
Pseudomonadota |
Bacteria
|
gut microbe |
- | ||
Kluyvera georgiana ATCC 516None3
Pseudomonadota |
Bacteria
|
gut microbe |
- | ||
Lactococcus lactis NBRC 1NoneNone933
Bacillota |
Bacteria
|
gut microbe |
- | ||
Lysinibacillus fusiformis NBRC 15717
Bacillota |
Bacteria
|
gut microbe |
- | ||
Pseudomonas citronellolis NBRC 1None3None43
Pseudomonadota |
Bacteria
|
gut microbe |
- | ||
Bacteria
|
gut microbe |
- | |||
Staphylococcus hominis GTC 1228
Bacillota |
Bacteria
|
gut microbe |
- | ||
Bacteria
|
gut microbe |
- | |||
T richoderma virens DAOM 164916
Ascomycota |
Fungi
|
gut microbe |
- | ||
Ambrosiella cleistominuta
Ascomycota |
Fungi
|
- |
- | ||
Ambrosiella roeperi
Ascomycota |
Fungi
|
- |
- | ||
Ambrosiella roeperi
Ascomycota |
Fungi
|
- |
- | ||
Ambrosiella xylebori
Ascomycota |
Fungi
|
- |
- | ||
bacteria
- |
Bacteria
|
- |
- | ||
bacteria
- |
Bacteria
|
- |
- | ||
bacteria
- |
Bacteria
|
- |
- | ||
bacteria
- |
Bacteria
|
- |
- | ||
bacteria
- |
Bacteria
|
- |
- | ||
bacteria
- |
Bacteria
|
- |
- | ||
bacteria
- |
Bacteria
|
- |
- | ||
bacteria
- |
Bacteria
|
- |
- | ||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria and Fungi
|
- |
- | |||
Bacteria
|
- |
- | |||
Burkholderia
Pseudomonadota |
Bacteria
|
- |
- | ||
Burkholderia gladioli Lv-StB
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Curculioniphilus buchneri
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Curculioniphilus buchneri
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Curculioniphilus buchneri
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Curculioniphilus buchneri
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Dasytiphilus stammeri
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Dasytiphilus stammeri
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Hodgkinia cicadicola like
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Macropleicola appendiculatae
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Macropleicola appendiculatae
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Macropleicola muticae
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Nardonella
Pseudomonadota |
Bacteria
|
- |
- | ||
Candidatus Sulcia muelleri
Bacteroidota |
Bacteria
|
- |
- | ||
Curculioniphilus
Pseudomonadota |
Bacteria
|
- |
- | ||
Dysgonomonas
Bacteroidota |
Bacteria
|
- |
- | ||
Endoconidiophora
Ascomycota |
Fungi
|
- |
- | ||
Enterobacteriaceae
Pseudomonadota |
Bacteria
|
- |
- | ||
Entomoplasmataceae
Mycoplasmatota |
Bacteria
|
- |
- | ||
Flavobacteriales
Bacteroidota |
Bacteria
|
- |
- | ||
Fusarium akasia
Ascomycota |
Fungi
|
- |
- | ||
Fusarium awan
Ascomycota |
Fungi
|
- |
- | ||
Fusarium mekan
Ascomycota |
Fungi
|
- |
- | ||
Fusarium rekanum sp. Nov
Ascomycota |
Fungi
|
- |
- | ||
Fusarium solani
Ascomycota |
Fungi
|
- |
- | ||
Fusarium sp.
Ascomycota |
Fungi
|
- |
- | ||
Fusarium variousi
Ascomycota |
Fungi
|
- |
- | ||
Fusarium warna
Ascomycota |
Fungi
|
- |
- | ||
Bacteria
|
- |
- | |||
Grosmannia clavigera
Ascomycota |
Fungi
|
- |
- | ||
Grosmannia clavigera
Ascomycota |
Fungi
|
- |
- | ||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria and Fungi
|
- |
- | |||
Fungi
|
- |
- | |||
Kodamaea ohmeri
Ascomycota |
Fungi
|
- |
- | ||
Lactobacillaceae
Bacillota |
Bacteria
|
- |
- | ||
Leptographium procerum
Ascomycota |
Fungi
|
- |
- | ||
Leptographium sanjiangyuanense sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Leptographium zekuense sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Micromonospora harpali sp. nov.
Actinomycetota |
Bacteria
|
- |
- | ||
Bacteria
|
- |
- | |||
Nardonella
Pseudomonadota |
Bacteria
|
- |
- | ||
Nardonella
Pseudomonadota |
Bacteria
|
- |
- | ||
Nardonella
Pseudomonadota |
Bacteria
|
- |
- | ||
Nardonella
Pseudomonadota |
Bacteria
|
- |
- | ||
Nardonella
Pseudomonadota |
Bacteria
|
- |
- | ||
Nardonella
Pseudomonadota |
Bacteria
|
- |
- | ||
Nardonella
Pseudomonadota |
Bacteria
|
- |
- | ||
Ophiostoma huangnanense sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma maixiuense sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma montium
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma sanum sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma sp.
Ascomycota |
Fungi
|
- |
- | ||
Pantoea agglomerans
Pseudomonadota |
Bacteria
|
- |
- | ||
Raffaelea quercina sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Rahnella
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Rickettsia
Pseudomonadota |
Bacteria
|
- |
- | ||
Sarocladium strictum
Ascomycota |
Fungi
|
- |
- | ||
Serratia
Pseudomonadota |
Bacteria
|
- |
- | ||
Serratia grimesii
Pseudomonadota |
Bacteria
|
- |
- | ||
Sodalis
Pseudomonadota |
Bacteria
|
- |
- | ||
Sodalis
Pseudomonadota |
Bacteria
|
- |
- | ||
Sodalis pierantonius
Pseudomonadota |
Bacteria
|
- |
- | ||
Spiroplasma
Mycoplasmatota |
Bacteria
|
- |
- | ||
Spiroplasma
Mycoplasmatota |
Bacteria
|
- |
- | ||
Spiroplasma
Mycoplasmatota |
Bacteria
|
- |
- | ||
Staphylococcus
Bacillota |
Bacteria
|
- |
- | ||
Staphylococcus
Bacillota |
Bacteria
|
- |
- | ||
Streptococcaceae
Bacillota |
Bacteria
|
- |
- | ||
Wolbachia
Pseudomonadota |
Bacteria
|
- |
- | ||
Wolbachia
Pseudomonadota |
Bacteria
|
- |
- | ||
Wolbachia
Pseudomonadota |
Bacteria
|
- |
- | ||
Wolbachia
Pseudomonadota |
Bacteria
|
- |
- | ||
Wolbachia ST375
Pseudomonadota |
Bacteria
|
- |
- | ||
Wolbachia wTcon
Pseudomonadota |
Bacteria
|
- |
- |
Metagenome Information
522 recordsMetagenome sequencing data associated with Coleoptera order
Run | Platform | Host | Location | Date | BioProject |
---|---|---|---|---|---|
DRR252954
WGS |
ILLUMINA
Illumina MiSeq |
-
|
NA
|
PRJDB10724 | |
DRR226615
WGS |
ILLUMINA
Illumina MiSeq |
Viet Nam
|
NA
|
PRJDB9773 | |
DRR414867
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Japan
|
NA
|
PRJDB14662 | |
DRR226614
WGS |
ILLUMINA
Illumina MiSeq |
Japan
|
NA
|
PRJDB9773 | |
DRR252955
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
-
|
NA
|
PRJDB10724 | |
SRR25394229
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Taiwan
22.3927 N 120.335 E |
2022/7/20
|
PRJNA997560 | |
SRR22520359
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
|
2022-10
|
PRJNA907216 | |
SRR22520360
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
|
2022-10
|
PRJNA907216 | |
SRR22520363
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
|
2022-10
|
PRJNA907216 | |
SRR22520358
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
|
2022-10
|
PRJNA907216 | |
SRR22520362
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
|
2022-10
|
PRJNA907216 | |
SRR22520361
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
|
2022-10
|
PRJNA907216 | |
SRR27811466
WGS |
ILLUMINA
NextSeq 2000 |
USA
45.25880 N 119.88716 W |
2022
|
PRJNA1068458 | |
SRR27811467
WGS |
ILLUMINA
NextSeq 2000 |
USA
45.25880 N 119.88716 W |
2022
|
PRJNA1068458 | |
SRR27811437
WGS |
ILLUMINA
NextSeq 2000 |
Germany
50.910548 N 11.567098 E |
2022
|
PRJNA1068458 | |
SRR27811436
WGS |
ILLUMINA
NextSeq 2000 |
Germany
50.910548 N 11.567098 E |
2022
|
PRJNA1068458 | |
SRR27811435
WGS |
ILLUMINA
NextSeq 2000 |
Germany
50.910548 N 11.567098 E |
2022
|
PRJNA1068458 | |
SRR27811468
WGS |
ILLUMINA
NextSeq 2000 |
USA
45.25880 N 119.88716 W |
2022
|
PRJNA1068458 | |
SRR27811469
WGS |
ILLUMINA
NextSeq 2000 |
USA
45.25880 N 119.88716 W |
2022
|
PRJNA1068458 | |
SRR23622344
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622334
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622335
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622336
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622337
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622338
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622339
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622340
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622341
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622342
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622343
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622345
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622346
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622347
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622348
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622349
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622350
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR23622351
WGS |
ILLUMINA
Illumina HiSeq 4000 |
Germany
48.53 N 9.05 E |
2021-10
|
PRJNA938905 | |
SRR27812167
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.73446 N 117.84770 W |
2021
|
PRJNA1068458 | |
SRR27812168
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.73446 N 117.84770 W |
2021
|
PRJNA1068458 | |
SRR27812169
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.73446 N 117.84770 W |
2021
|
PRJNA1068458 | |
SRR27812170
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.73446 N 117.84770 W |
2021
|
PRJNA1068458 | |
SRR19201368
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
|
2020-08-08
|
PRJNA836854 | |
SRR24210634
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
35.3275 N 101.9361 E |
2020-07
|
PRJNA956988 | |
SRR24210635
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
35.3275 N 101.9361 E |
2020-07
|
PRJNA956988 | |
SRR24210636
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
35.3275 N 101.9361 E |
2020-07
|
PRJNA956988 | |
SRR24210637
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
35.3275 N 101.9361 E |
2020-07
|
PRJNA956988 | |
SRR24210638
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
35.3275 N 101.9361 E |
2020-07
|
PRJNA956988 | |
SRR24210639
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
China
35.3275 N 101.9361 E |
2020-07
|
PRJNA956988 | |
SRR19201388
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
|
2020-06-21
|
PRJNA836854 | |
SRR19201360
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
|
2020-04-26
|
PRJNA836854 | |
SRR27874669
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.660197 N 7.985386 E |
2020
|
PRJNA1072544 | |
SRR19201373
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Czech Republic
|
2020
|
PRJNA836854 | |
SRR19201376
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
|
2020
|
PRJNA836854 | |
SRR19201379
WGS |
ILLUMINA
Illumina HiSeq 3000 |
New Zealand
|
2020
|
PRJNA836854 | |
SRR27874688
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874689
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874690
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.660197 N 7.985386 E |
2020
|
PRJNA1072544 | |
SRR27874691
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874692
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874693
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874694
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874695
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874696
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874697
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874698
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874699
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874700
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874701
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.660197 N 7.985386 E |
2020
|
PRJNA1072544 | |
SRR27874702
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.660197 N 7.985386 E |
2020
|
PRJNA1072544 | |
SRR27874680
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.853770 N 8.377150 E |
2020
|
PRJNA1072544 | |
SRR27874679
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.660197 N 7.985386 E |
2020
|
PRJNA1072544 | |
SRR27874681
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.853770 N 8.377150 E |
2020
|
PRJNA1072544 | |
SRR27874682
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874683
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874684
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874685
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR28034353
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
43.023083 N 141.416590 E |
2020
|
PRJNA1062330 | |
SRR28034354
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
43.023083 N 141.416590 E |
2020
|
PRJNA1062330 | |
SRR28034355
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
43.023083 N 141.416590 E |
2020
|
PRJNA1062330 | |
SRR28034356
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
43.023083 N 141.416590 E |
2020
|
PRJNA1062330 | |
SRR28034357
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
43.023083 N 141.416590 E |
2020
|
PRJNA1062330 | |
SRR27874678
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.853770 N 8.377150 E |
2020
|
PRJNA1072544 | |
SRR28034359
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
43.023083 N 141.416590 E |
2020
|
PRJNA1062330 | |
SRR28034360
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
43.023083 N 141.416590 E |
2020
|
PRJNA1062330 | |
SRR28034361
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
43.023083 N 141.416590 E |
2020
|
PRJNA1062330 | |
SRR27874686
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874687
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874677
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.853770 N 8.377150 E |
2020
|
PRJNA1072544 | |
SRR27874671
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.660197 N 7.985386 E |
2020
|
PRJNA1072544 | |
SRR27874670
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.660197 N 7.985386 E |
2020
|
PRJNA1072544 | |
SRR27874668
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.660197 N 7.985386 E |
2020
|
PRJNA1072544 | |
SRR27874667
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27874666
WGS |
ILLUMINA
NextSeq 2000 |
Germany
49.604754 N 8.236137 E |
2020
|
PRJNA1072544 | |
SRR27811434
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Italy
43.955000 N 8.123333 E |
2020
|
PRJNA1068458 | |
SRR27811433
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Italy
43.955000 N 8.123333 E |
2020
|
PRJNA1068458 | |
SRR14139298
WGS |
ILLUMINA
HiSeq X Ten |
China
29.38 N 103.30 E |
2019-07-15
|
PRJNA719486 | |
SRR14139297
WGS |
ILLUMINA
HiSeq X Ten |
China
29.38 N 103.30 E |
2019-07-15
|
PRJNA719486 | |
SRR14139296
WGS |
ILLUMINA
HiSeq X Ten |
China
29.38 N 103.30 E |
2019-07-15
|
PRJNA719486 | |
SRR14139293
WGS |
ILLUMINA
HiSeq X Ten |
China
29.38 N 103.30 E |
2019-07-15
|
PRJNA719486 | |
SRR14139294
WGS |
ILLUMINA
HiSeq X Ten |
China
29.38 N 103.30 E |
2019-07-15
|
PRJNA719486 | |
SRR14139295
WGS |
ILLUMINA
HiSeq X Ten |
China
29.38 N 103.30 E |
2019-07-15
|
PRJNA719486 | |
SRR28034347
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Germany
50.922011 N 11.585965 E |
2019
|
PRJNA1062330 | |
SRR28034346
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
50.922011 N 11.585965 E |
2019
|
PRJNA1062330 | |
SRR28034348
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Belgium
50.026488 N 4.622770 E |
2019
|
PRJNA1062330 | |
SRR28034349
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Belgium
50.026488 N 4.622770 E |
2019
|
PRJNA1062330 | |
SRR28034350
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Belgium
50.026488 N 4.622770 E |
2019
|
PRJNA1062330 | |
SRR28034351
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Belgium
50.026488 N 4.622770 E |
2019
|
PRJNA1062330 | |
SRR28034352
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Belgium
50.026488 N 4.622770 E |
2019
|
PRJNA1062330 | |
SRR28113948
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Belgium
50.026488 N 4.622770 E |
2019
|
PRJNA1062330 | |
SRR28113947
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Belgium
50.026488 N 4.622770 E |
2019
|
PRJNA1062330 | |
SRR27811357
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Germany
49.990637 N 8.239281 E |
2019
|
PRJNA1068458 | |
SRR27811358
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Germany
49.546648 N 8.075657 E |
2019
|
PRJNA1068458 | |
SRR27811899
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.39172 N 117.62987 W |
2019
|
PRJNA1068458 | |
SRR27811900
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.39172 N 117.62987 W |
2019
|
PRJNA1068458 | |
SRR27811901
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.39172 N 117.62987 W |
2019
|
PRJNA1068458 | |
SRR27811902
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.39172 N 117.62987 W |
2019
|
PRJNA1068458 | |
SRR27812163
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Germany
49.990637 N 8.239281 E |
2019
|
PRJNA1068458 | |
SRR27829352
WGS |
ILLUMINA
NextSeq 2000 |
USA
31.93314 N 109.26383 W |
2019
|
PRJNA1068458 | |
SRR27829353
WGS |
ILLUMINA
NextSeq 2000 |
USA
31.93314 N 109.26383 W |
2019
|
PRJNA1068458 | |
SRR27829354
WGS |
ILLUMINA
NextSeq 2000 |
USA
31.93314 N 109.26383 W |
2019
|
PRJNA1068458 | |
SRR27829355
WGS |
ILLUMINA
NextSeq 2000 |
USA
31.93314 N 109.26383 W |
2019
|
PRJNA1068458 | |
SRR12668521
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-08-24
|
PRJNA663749 | |
SRR12668522
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-08-24
|
PRJNA663749 | |
SRR12668520
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-08-24
|
PRJNA663749 | |
SRR12668523
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-31
|
PRJNA663749 | |
SRR12668524
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-31
|
PRJNA663749 | |
SRR12668452
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668460
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668478
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668477
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668476
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668474
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668473
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668472
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668471
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668470
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668469
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668468
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668467
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668466
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668465
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668459
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668491
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668463
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668462
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668461
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668490
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668489
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668458
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668457
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668456
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668455
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR12668454
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-07-24
|
PRJNA663749 | |
SRR19201361
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
|
2018-07-01
|
PRJNA836854 | |
SRR19201367
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
|
2018-07-01
|
PRJNA836854 | |
SRR19201358
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
|
2018-07-01
|
PRJNA836854 | |
SRR12668544
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668528
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668496
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668495
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668501
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668500
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668546
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668536
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668535
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668534
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668446
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668545
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668529
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668515
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668527
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668526
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668494
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668479
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668480
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668498
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668497
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668447
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668509
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668508
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668507
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668482
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668504
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668449
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR12668502
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2018-02-05
|
PRJNA663749 | |
SRR27874672
WGS |
OXFORD_NANOPORE
MinION |
Germany
50.871 N 10.500 E |
2018
|
PRJNA1072544 | |
SRR27874673
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
50.871 N 10.500 E |
2018
|
PRJNA1072544 | |
SRR27811903
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.52186 N 119.83201 W |
2018
|
PRJNA1068458 | |
SRR27811904
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.52186 N 119.83201 W |
2018
|
PRJNA1068458 | |
SRR27811905
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.52186 N 119.83201 W |
2018
|
PRJNA1068458 | |
SRR27811906
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.52186 N 119.83201 W |
2018
|
PRJNA1068458 | |
SRR27811406
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.429550 N 118.112180 W |
2018
|
PRJNA1068458 | |
SRR27811407
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.429550 N 118.112180 W |
2018
|
PRJNA1068458 | |
SRR27829362
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.17984 N 118.09790 W |
2018
|
PRJNA1068458 | |
SRR28034358
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Germany
49.993330 N 8.243941 E |
2018
|
PRJNA1062330 | |
SRR27874674
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
50.871 N 10.500 E |
2018
|
PRJNA1072544 | |
SRR27811405
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.429550 N 118.112180 W |
2018
|
PRJNA1068458 | |
SRR27811404
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
34.429550 N 118.112180 W |
2018
|
PRJNA1068458 | |
SRR27829359
WGS |
OXFORD_NANOPORE
MinION |
USA
34.17984 N 118.09790 W |
2018
|
PRJNA1068458 | |
SRR27829361
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.17984 N 118.09790 W |
2018
|
PRJNA1068458 | |
SRR27829360
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.17984 N 118.09790 W |
2018
|
PRJNA1068458 | |
SRR27829358
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.17984 N 118.09790 W |
2018
|
PRJNA1068458 | |
SRR12668443
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668444
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668445
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668448
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668450
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668451
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668453
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668464
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668475
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668481
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668483
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668484
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668485
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668486
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668487
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668488
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668492
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668493
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668499
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668503
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668505
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668510
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668511
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668512
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668513
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668514
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668516
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668517
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668518
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668519
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668525
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668530
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668531
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668532
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668533
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668537
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668538
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668539
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668540
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668541
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668542
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668543
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668547
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668548
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR12668549
WGS |
ILLUMINA
Illumina MiSeq |
India
12.9716 N 77.5946 E |
2017-08-12
|
PRJNA663749 | |
SRR10017628
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Japan
35.6762 N 139.6503 E |
2017-05-01
|
PRJNA561424 | |
SRR10017631
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Germany
50.9271 N 11.5892 E |
2017-05-01
|
PRJNA561424 | |
SRR10017626
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Panama
8.9824 N 79.5199 W |
2017-05-01
|
PRJNA561424 | |
SRR10017629
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Panama
8.9824 N 79.5199 W |
2017-05-01
|
PRJNA561424 | |
SRR10017630
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Panama
8.9824 N 79.5199 W |
2017-05-01
|
PRJNA561424 | |
SRR10017625
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Panama
8.9824 N 79.5199 W |
2017-05-01
|
PRJNA561424 | |
SRR10017632
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Germany
50.9271 N 11.5892 E |
2017-05-01
|
PRJNA561424 | |
SRR10017622
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Panama
8.9824 N 79.5199 W |
2017-05-01
|
PRJNA561424 | |
SRR10017624
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Panama
8.9824 N 79.5199 W |
2017-05-01
|
PRJNA561424 | |
SRR10017621
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Panama
8.9824 N 79.5199 W |
2017-05-01
|
PRJNA561424 | |
SRR10017627
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Panama
8.9824 N 79.5199 W |
2017-05-01
|
PRJNA561424 | |
SRR24296966
WGS |
ILLUMINA
NextSeq 550 |
USA
not collected |
2017-02-15
|
PRJNA961367 | |
SRR24296967
WGS |
ILLUMINA
NextSeq 550 |
USA
not collected |
2017-02-15
|
PRJNA961367 | |
SRR24296964
WGS |
ILLUMINA
NextSeq 550 |
USA
not collected |
2017-02-15
|
PRJNA961367 | |
SRR24296965
WGS |
ILLUMINA
NextSeq 550 |
USA
not collected |
2017-02-15
|
PRJNA961367 | |
SRR27829356
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
USA
34.53352 N 120.04031 W |
2017
|
PRJNA1068458 | |
SRR27811432
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
USA
34.07659 N 118.68803 W |
2017
|
PRJNA1068458 | |
SRR27811465
WGS |
ILLUMINA
NextSeq 2000 |
USA
39.79193 N 111.67870 W |
2017
|
PRJNA1068458 | |
SRR27811464
WGS |
ILLUMINA
NextSeq 2000 |
USA
39.79193 N 111.67870 W |
2017
|
PRJNA1068458 | |
SRR27811463
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.51160 N 120.50212 W |
2017
|
PRJNA1068458 | |
SRR27811462
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.51160 N 120.50212 W |
2017
|
PRJNA1068458 | |
SRR27811461
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.51160 N 120.50212 W |
2017
|
PRJNA1068458 | |
SRR27811460
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.51160 N 120.50212 W |
2017
|
PRJNA1068458 | |
SRR27829357
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
USA
34.53352 N 120.04031 W |
2017
|
PRJNA1068458 | |
SRR27811473
WGS |
ILLUMINA
NextSeq 2000 |
USA
39.79193 N 111.67870 W |
2017
|
PRJNA1068458 | |
SRR27811472
WGS |
ILLUMINA
NextSeq 2000 |
USA
39.79193 N 111.67870 W |
2017
|
PRJNA1068458 | |
SRR19201370
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
|
2016-09-12
|
PRJNA836854 | |
SRR19201369
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Germany
|
2016-05-01
|
PRJNA836854 | |
SRR19201355
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Japan
|
2016-04-12
|
PRJNA836854 | |
SRR19201354
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
|
2016-04-12
|
PRJNA836854 | |
SRR19201362
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Germany
|
2016-04-01
|
PRJNA836854 | |
SRR19201387
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Japan
|
2016-03-18
|
PRJNA836854 | |
SRR5626971
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384399 | |
SRR5626976
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384388 | |
SRR5626975
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384388 | |
SRR5626974
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384399 | |
SRR5626973
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384399 | |
SRR5626972
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384399 | |
SRR5626970
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384399 | |
SRR5626969
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384399 | |
SRR5626968
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384399 | |
SRR5626967
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384399 | |
SRR6147586
WGS |
ILLUMINA
Illumina HiSeq 2500 |
New Zealand
40.9006 S 174.8860 E |
2016
|
PRJNA413589 | |
SRR27811471
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.67448 N 118.39446 W |
2016
|
PRJNA1068458 | |
SRR27811470
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.67448 N 118.39446 W |
2016
|
PRJNA1068458 | |
SRR5626982
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384388 | |
SRR27811459
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.67448 N 118.39446 W |
2016
|
PRJNA1068458 | |
SRR27811458
WGS |
ILLUMINA
NextSeq 2000 |
USA
34.67448 N 118.39446 W |
2016
|
PRJNA1068458 | |
SRR5626981
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384388 | |
SRR5626980
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384388 | |
SRR5626979
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384388 | |
SRR5626978
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384388 | |
SRR5626977
WGS |
ILLUMINA
Illumina HiSeq 2500 |
USA
44.9905 N 93.1805 W |
2016
|
PRJNA384388 | |
SRR13786458
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786461
WGS |
ILLUMINA
Illumina MiSeq |
France
43.703736 N 3.858611 E |
2015-04-01
|
PRJNA704818 | |
SRR13786462
WGS |
ILLUMINA
Illumina MiSeq |
France
43.703736 N 3.858611 E |
2015-04-01
|
PRJNA704818 | |
SRR13786463
WGS |
ILLUMINA
Illumina MiSeq |
France
43.703736 N 3.858611 E |
2015-04-01
|
PRJNA704818 | |
SRR13786464
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786465
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786466
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786451
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786456
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786455
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786454
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786453
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786452
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR13786457
WGS |
ILLUMINA
Illumina MiSeq |
France
43.705043 N 3.863410 E |
2015-04-01
|
PRJNA704818 | |
SRR5342668
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR19201357
WGS |
OXFORD_NANOPORE
MinION |
Germany
|
2015
|
PRJNA836854 | |
SRR27811413
WGS |
ILLUMINA
NextSeq 2000 |
Italy
46.83752 N 12.10405 E |
2015
|
PRJNA1068458 | |
SRR27811412
WGS |
ILLUMINA
NextSeq 2000 |
Italy
46.83752 N 12.10405 E |
2015
|
PRJNA1068458 | |
SRR27811411
WGS |
ILLUMINA
NextSeq 2000 |
Italy
46.83752 N 12.10405 E |
2015
|
PRJNA1068458 | |
SRR27874676
WGS |
ILLUMINA
NextSeq 2000 |
Germany
48.030139 N 11.350212 E |
2015
|
PRJNA1072544 | |
SRR27874675
WGS |
ILLUMINA
NextSeq 2000 |
Germany
48.030139 N 11.350212 E |
2015
|
PRJNA1072544 | |
SRR19201365
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
|
2015
|
PRJNA836854 | |
SRR5350655
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350656
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5342614
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342615
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342616
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342617
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342618
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342619
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342620
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342621
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342622
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342623
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342624
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342625
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342626
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342628
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377711 | |
SRR5342660
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342661
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342662
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342663
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342664
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342665
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342666
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342667
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342669
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342670
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342671
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342672
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342674
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377641 | |
SRR5342693
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377639 | |
SRR5342694
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377639 | |
SRR5342695
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377639 | |
SRR5342696
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377639 | |
SRR5342704
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377633 | |
SRR5342705
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377633 | |
SRR5342707
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377633 | |
SRR5342708
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377633 | |
SRR5342709
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377633 | |
SRR5342710
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377633 | |
SRR5342714
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377582 | |
SRR5342715
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377582 | |
SRR5342716
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377582 | |
SRR5651489
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
11.8602 S 55.6222 W |
2015
|
PRJNA385329 | |
SRR5644309
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
11.8602 S 55.6222 W |
2015
|
PRJNA384877 | |
SRR5350637
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350638
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350639
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350640
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350641
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350643
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350645
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350646
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350647
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350648
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350649
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350650
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350651
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350652
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350653
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR5350654
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Brazil
15.73 S 47.9002 W |
2015
|
PRJNA377714 | |
SRR14161588
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14147653
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14161469
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14177633
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14224883
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA721277 | |
SRR14179764
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14139157
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14179698
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14179697
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14139180
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14212118
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA721277 | |
SRR14209386
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14161071
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14162401
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14160491
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14139235
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14160440
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR5038971
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA354118 | |
SRR5039436
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA354118 | |
SRR14300306
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA721277 | |
SRR14298725
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA721277 | |
SRR14298063
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA721277 | |
SRR14141452
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14141486
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14141637
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14141657
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14141706
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14141739
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14141816
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14141829
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR5039445
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA354118 | |
SRR14128221
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719072 | |
SRR14132028
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719072 | |
SRR14132050
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719072 | |
SRR14293692
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA721277 | |
SRR14193501
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA720473 | |
SRR14193931
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA720473 | |
SRR14180362
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14180364
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14180536
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14150473
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14149805
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14149278
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR14148842
RNA-Seq |
ILLUMINA
Illumina HiSeq 2500 |
China
|
2014/10/30
|
PRJNA719476 | |
SRR19201386
WGS |
OXFORD_NANOPORE
MinION |
Germany
|
2014
|
PRJNA836854 | |
SRR28034368
WGS |
ILLUMINA
NextSeq 2000 |
Germany
51.310948 N 11.191484 E |
2014
|
PRJNA1062330 | |
SRR28034366
WGS |
ILLUMINA
NextSeq 2000 |
Germany
51.310948 N 11.191484 E |
2014
|
PRJNA1062330 | |
SRR27811911
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Canada
49.301 N 123.14 W |
2014
|
PRJNA1062330 | |
SRR27811910
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Canada
49.301 N 123.14 W |
2014
|
PRJNA1062330 | |
SRR27811909
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Canada
49.301 N 123.14 W |
2014
|
PRJNA1062330 | |
SRR27811908
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Canada
49.301 N 123.14 W |
2014
|
PRJNA1062330 | |
SRR19201352
WGS |
OXFORD_NANOPORE
MinION |
Germany
|
2014
|
PRJNA836854 | |
SRR19201385
WGS |
PACBIO_SMRT
Sequel II |
Germany
|
2014
|
PRJNA836854 | |
SRR28034367
WGS |
ILLUMINA
NextSeq 2000 |
Germany
51.310948 N 11.191484 E |
2014
|
PRJNA1062330 | |
SRR27811410
WGS |
ILLUMINA
NextSeq 2000 |
Germany
51.870740 N 10.999714 E |
2014
|
PRJNA1068458 | |
SRR27811409
WGS |
ILLUMINA
NextSeq 2000 |
Germany
51.870740 N 10.999714 E |
2014
|
PRJNA1068458 | |
SRR19201353
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Germany
|
2014
|
PRJNA836854 | |
SRR19201356
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Germany
|
2014
|
PRJNA836854 | |
SRR27811408
WGS |
ILLUMINA
NextSeq 2000 |
Germany
51.870740 N 10.999714 E |
2014
|
PRJNA1068458 | |
SRR19201380
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Germany
|
2014
|
PRJNA836854 | |
SRR19201381
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Germany
|
2014
|
PRJNA836854 | |
SRR19201382
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Germany
|
2014
|
PRJNA836854 | |
SRR19201383
WGS |
ILLUMINA
Illumina NovaSeq 6000 |
Germany
|
2014
|
PRJNA836854 | |
SRR19201384
WGS |
ILLUMINA
Illumina HiSeq 2500 |
Germany
|
2014
|
PRJNA836854 | |
SRR22996347
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996348
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996349
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996350
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996351
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996352
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996343
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996353
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996354
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996355
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996356
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996357
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996344
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996345
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996346
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996342
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996341
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996340
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996339
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996338
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996337
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996336
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996335
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996334
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996333
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996328
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR22996327
RNA-Seq |
ILLUMINA
Illumina HiSeq 4000 |
France
|
2011/12/1
|
PRJNA918957 | |
SRR23250343
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250344
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250345
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250350
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250351
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250339
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250316
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250317
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250318
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250319
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250320
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250321
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250322
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250323
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250324
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250325
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250326
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250327
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250328
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250329
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250330
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250331
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250332
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250333
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250334
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250335
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250336
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250337
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250338
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250340
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250341
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR23250342
OTHER |
ILLUMINA
NextSeq 500 |
France
|
2011
|
PRJNA918957 | |
SRR27812164
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
51.826361 N 12.042761 E |
2011
|
PRJNA1068458 | |
SRR27812165
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
51.826361 N 12.042761 E |
2011
|
PRJNA1068458 | |
SRR27812166
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Germany
51.826361 N 12.042761 E |
2011
|
PRJNA1068458 | |
SRR28034369
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Australia
26.890000 S 151.616000 E |
2010
|
PRJNA1062330 | |
SRR28034370
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Australia
26.890000 S 151.616000 E |
2010
|
PRJNA1062330 | |
SRR19201377
WGS |
ILLUMINA
Illumina HiSeq 3000 |
United Arab Emirates
|
2006-03-22
|
PRJNA836854 | |
SRR19201359
WGS |
ILLUMINA
Illumina HiSeq 3000 |
United Arab Emirates
|
2005-06-05
|
PRJNA836854 | |
SRR28034363
WGS |
ILLUMINA
NextSeq 2000 |
USA
36.0773 N 121.5940 W |
2004
|
PRJNA1062330 | |
SRR28034365
WGS |
ILLUMINA
NextSeq 2000 |
USA
36.0773 N 121.5940 W |
2004
|
PRJNA1062330 | |
SRR28034362
WGS |
ILLUMINA
NextSeq 2000 |
USA
36.0773 N 121.5940 W |
2004
|
PRJNA1062330 | |
SRR28034364
WGS |
ILLUMINA
NextSeq 2000 |
USA
36.0773 N 121.5940 W |
2004
|
PRJNA1062330 | |
SRR19201372
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Yemen
|
2001-09-15
|
PRJNA836854 | |
SRR19201363
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Yemen
|
2001-07-12
|
PRJNA836854 | |
SRR19201375
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
|
1994
|
PRJNA836854 | |
SRR19201371
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Yemen
|
1992-08-01
|
PRJNA836854 | |
SRR19201378
WGS |
ILLUMINA
Illumina HiSeq 3000 |
Yemen
|
1992-06-29
|
PRJNA836854 | |
SRR19201374
WGS |
ILLUMINA
Illumina HiSeq 3000 |
USA
|
1988-06-15
|
PRJNA836854 |
Amplicon Information
951 recordsAmplicon sequencing data associated with Coleoptera order
Run | Classification | Host | Platform | Location | Environment |
---|---|---|---|---|---|
SRR20075036
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075025
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075026
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075027
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075028
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075029
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075030
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075031
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075032
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075033
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075034
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR20075035
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR11426213
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426214
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426215
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426216
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426217
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426218
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426219
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426220
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426222
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426223
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426224
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426225
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426226
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426227
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426228
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426229
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426230
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426231
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426232
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426233
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426234
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426235
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426236
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426237
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426238
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426239
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426240
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426241
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426242
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426243
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426244
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426245
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426246
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426247
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426248
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426221
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426202
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426203
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426204
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426205
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426206
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426207
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426208
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426209
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426210
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426211
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426212
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR11426201
AMPLICON |
16S
|
-
|
uncalculated
|
-
|
|
SRR25992754
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992737
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992738
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992739
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992740
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992741
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992742
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992743
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992744
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992745
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992746
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992747
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992748
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992749
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992750
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992751
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992752
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992761
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992760
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992759
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992758
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992757
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992756
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992755
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR25992753
AMPLICON |
16S
|
-
|
China
30 N 120 E |
-
|
|
SRR17438330
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438335
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438334
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438333
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438332
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438331
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438329
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438328
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438327
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438326
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR17438325
AMPLICON |
16S
|
-
|
India
not applicable |
-
|
|
SRR25457017
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457019
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457020
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457021
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457022
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457023
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457024
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457025
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457026
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457027
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457028
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457010
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457011
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457012
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457013
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457014
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457015
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457016
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457018
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457029
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR25457030
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR27416538
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416539
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416540
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416541
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416543
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416544
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416584
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416585
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416586
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416587
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416588
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416590
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416591
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416592
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416593
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416595
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416596
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416597
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416598
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416599
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416601
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416602
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416603
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416604
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416605
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416606
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416607
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416608
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416609
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416610
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416644
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416645
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416646
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416647
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416648
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416649
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416650
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416651
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416652
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416655
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416656
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416657
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416658
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416659
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416660
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR21053560
AMPLICON |
16S and ITS
|
-
|
Kenya
1.13 S 36.53 E |
ENVO:02000022
ENVO:00002003 |
|
SRR21053556
AMPLICON |
16S and ITS
|
-
|
Kenya
1.13 S 36.53 E |
ENVO:02000022
ENVO:00002003 |
|
SRR27416669
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416668
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416667
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416666
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416664
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416663
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416662
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416661
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR25774112
AMPLICON |
16S
|
-
|
China
31.14 N 118.83 E |
-
|
|
SRR25774095
AMPLICON |
16S
|
-
|
China
31.14 N 118.99 E |
-
|
|
SRR25774096
AMPLICON |
16S
|
-
|
China
31.14 N 118.98 E |
-
|
|
SRR25774097
AMPLICON |
16S
|
-
|
China
31.14 N 118.97 E |
-
|
|
SRR25774098
AMPLICON |
16S
|
-
|
China
31.14 N 118.96 E |
-
|
|
SRR25774076
AMPLICON |
16S
|
-
|
China
31.14 N 118.116 E |
-
|
|
SRR25774077
AMPLICON |
16S
|
-
|
China
31.14 N 118.115 E |
-
|
|
SRR25774078
AMPLICON |
16S
|
-
|
China
31.14 N 118.114 E |
-
|
|
SRR25774079
AMPLICON |
16S
|
-
|
China
31.14 N 118.113 E |
-
|
|
SRR25774080
AMPLICON |
16S
|
-
|
China
31.14 N 118.112 E |
-
|
|
SRR25774081
AMPLICON |
16S
|
-
|
China
31.14 N 118.31 E |
-
|
|
SRR25774082
AMPLICON |
16S
|
-
|
China
31.14 N 118.111 E |
-
|
|
SRR25774083
AMPLICON |
16S
|
-
|
China
31.14 N 118.110 E |
-
|
|
SRR25774084
AMPLICON |
16S
|
-
|
China
31.14 N 118.109 E |
-
|
|
SRR25774085
AMPLICON |
16S
|
-
|
China
31.14 N 118.108 E |
-
|
|
SRR25774086
AMPLICON |
16S
|
-
|
China
31.14 N 118.107 E |
-
|
|
SRR25774087
AMPLICON |
16S
|
-
|
China
31.14 N 118.106 E |
-
|
|
SRR25774088
AMPLICON |
16S
|
-
|
China
31.14 N 118.105 E |
-
|
|
SRR25774089
AMPLICON |
16S
|
-
|
China
31.14 N 118.104 E |
-
|
|
SRR25774090
AMPLICON |
16S
|
-
|
China
31.14 N 118.103 E |
-
|
|
SRR25774091
AMPLICON |
16S
|
-
|
China
31.14 N 118.102 E |
-
|
|
SRR25774092
AMPLICON |
16S
|
-
|
China
31.14 N 118.30 E |
-
|
|
SRR25774093
AMPLICON |
16S
|
-
|
China
31.14 N 118.101 E |
-
|
|
SRR25774094
AMPLICON |
16S
|
-
|
China
31.14 N 118.100 E |
-
|
|
SRR25774071
AMPLICON |
16S
|
-
|
China
31.14 N 118.121 E |
-
|
|
SRR25774072
AMPLICON |
16S
|
-
|
China
31.14 N 118.120 E |
-
|
|
SRR25774073
AMPLICON |
16S
|
-
|
China
31.14 N 118.119 E |
-
|
|
SRR25774074
AMPLICON |
16S
|
-
|
China
31.14 N 118.118 E |
-
|
|
SRR25774075
AMPLICON |
16S
|
-
|
China
31.14 N 118.117 E |
-
|
|
SRR25774099
AMPLICON |
16S
|
-
|
China
31.14 N 118.95 E |
-
|
|
SRR25774100
AMPLICON |
16S
|
-
|
China
31.14 N 118.94 E |
-
|
|
SRR25774101
AMPLICON |
16S
|
-
|
China
31.14 N 118.93 E |
-
|
|
SRR25774102
AMPLICON |
16S
|
-
|
China
31.14 N 118.92 E |
-
|
|
SRR25774103
AMPLICON |
16S
|
-
|
China
31.14 N 118.29 E |
-
|
|
SRR25774104
AMPLICON |
16S
|
-
|
China
31.14 N 118.91 E |
-
|
|
SRR25774105
AMPLICON |
16S
|
-
|
China
31.14 N 118.90 E |
-
|
|
SRR25774106
AMPLICON |
16S
|
-
|
China
31.14 N 118.89 E |
-
|
|
SRR25774107
AMPLICON |
16S
|
-
|
China
31.14 N 118.88 E |
-
|
|
SRR25774108
AMPLICON |
16S
|
-
|
China
31.14 N 118.87 E |
-
|
|
SRR25774109
AMPLICON |
16S
|
-
|
China
31.14 N 118.86 E |
-
|
|
SRR25774110
AMPLICON |
16S
|
-
|
China
31.14 N 118.85 E |
-
|
|
SRR25774111
AMPLICON |
16S
|
-
|
China
31.14 N 118.84 E |
-
|
|
SRR25774113
AMPLICON |
16S
|
-
|
China
31.14 N 118.82 E |
-
|
|
SRR25774114
AMPLICON |
16S
|
-
|
China
31.14 N 118.28 E |
-
|
|
SRR25774115
AMPLICON |
16S
|
-
|
China
31.14 N 118.81 E |
-
|
|
SRR25774116
AMPLICON |
16S
|
-
|
China
31.14 N 118.80 E |
-
|
|
SRR25774117
AMPLICON |
16S
|
-
|
China
31.14 N 118.79 E |
-
|
|
SRR25774118
AMPLICON |
16S
|
-
|
China
31.14 N 118.78 E |
-
|
|
SRR25774119
AMPLICON |
16S
|
-
|
China
31.14 N 118.77 E |
-
|
|
SRR25774120
AMPLICON |
16S
|
-
|
China
31.14 N 118.76 E |
-
|
|
SRR25774121
AMPLICON |
16S
|
-
|
China
31.14 N 118.75 E |
-
|
|
SRR25774122
AMPLICON |
16S
|
-
|
China
31.14 N 118.74 E |
-
|
|
SRR25774123
AMPLICON |
16S
|
-
|
China
31.14 N 118.73 E |
-
|
|
SRR25774124
AMPLICON |
16S
|
-
|
China
31.14 N 118.72 E |
-
|
|
SRR25774125
AMPLICON |
16S
|
-
|
China
31.14 N 118.27 E |
-
|
|
SRR25774126
AMPLICON |
16S
|
-
|
China
31.14 N 118.71 E |
-
|
|
SRR25774127
AMPLICON |
16S
|
-
|
China
31.14 N 118.70 E |
-
|
|
SRR25774128
AMPLICON |
16S
|
-
|
China
31.14 N 118.69 E |
-
|
|
SRR25774129
AMPLICON |
16S
|
-
|
China
31.14 N 118.68 E |
-
|
|
SRR25774130
AMPLICON |
16S
|
-
|
China
31.14 N 118.67 E |
-
|
|
SRR25774131
AMPLICON |
16S
|
-
|
China
31.14 N 118.66 E |
-
|
|
SRR25774132
AMPLICON |
16S
|
-
|
China
31.14 N 118.65 E |
-
|
|
SRR25774133
AMPLICON |
16S
|
-
|
China
31.14 N 118.64 E |
-
|
|
SRR25774134
AMPLICON |
16S
|
-
|
China
31.14 N 118.63 E |
-
|
|
SRR25774135
AMPLICON |
16S
|
-
|
China
31.14 N 118.62 E |
-
|
|
SRR25774136
AMPLICON |
16S
|
-
|
China
31.14 N 118.26 E |
-
|
|
SRR25774137
AMPLICON |
16S
|
-
|
China
31.14 N 118.61 E |
-
|
|
SRR25774138
AMPLICON |
16S
|
-
|
China
31.14 N 118.60 E |
-
|
|
SRR25774139
AMPLICON |
16S
|
-
|
China
31.14 N 118.59 E |
-
|
|
SRR25774140
AMPLICON |
16S
|
-
|
China
31.14 N 118.58 E |
-
|
|
SRR25774141
AMPLICON |
16S
|
-
|
China
31.14 N 118.57 E |
-
|
|
SRR25774142
AMPLICON |
16S
|
-
|
China
31.14 N 118.56 E |
-
|
|
SRR25774143
AMPLICON |
16S
|
-
|
China
31.14 N 118.55 E |
-
|
|
SRR25774144
AMPLICON |
16S
|
-
|
China
31.14 N 118.54 E |
-
|
|
SRR25774145
AMPLICON |
16S
|
-
|
China
31.14 N 118.53 E |
-
|
|
SRR25774146
AMPLICON |
16S
|
-
|
China
31.14 N 118.52 E |
-
|
|
SRR25774147
AMPLICON |
16S
|
-
|
China
31.14 N 118.25 E |
-
|
|
SRR25774148
AMPLICON |
16S
|
-
|
China
31.14 N 118.51 E |
-
|
|
SRR25774149
AMPLICON |
16S
|
-
|
China
31.14 N 118.50 E |
-
|
|
SRR25774150
AMPLICON |
16S
|
-
|
China
31.14 N 118.49 E |
-
|
|
SRR25774151
AMPLICON |
16S
|
-
|
China
31.14 N 118.48 E |
-
|
|
SRR25774152
AMPLICON |
16S
|
-
|
China
31.14 N 118.47 E |
-
|
|
SRR25774153
AMPLICON |
16S
|
-
|
China
31.14 N 118.46 E |
-
|
|
SRR25774154
AMPLICON |
16S
|
-
|
China
31.14 N 118.45 E |
-
|
|
SRR25774155
AMPLICON |
16S
|
-
|
China
31.14 N 118.44 E |
-
|
|
SRR25774156
AMPLICON |
16S
|
-
|
China
31.14 N 118.43 E |
-
|
|
SRR25774157
AMPLICON |
16S
|
-
|
China
31.14 N 118.42 E |
-
|
|
SRR25774158
AMPLICON |
16S
|
-
|
China
31.14 N 118.24 E |
-
|
|
SRR25774159
AMPLICON |
16S
|
-
|
China
31.14 N 118.41 E |
-
|
|
SRR25774160
AMPLICON |
16S
|
-
|
China
31.14 N 118.40 E |
-
|
|
SRR25774161
AMPLICON |
16S
|
-
|
China
31.14 N 118.39 E |
-
|
|
SRR25774162
AMPLICON |
16S
|
-
|
China
31.14 N 118.38 E |
-
|
|
SRR25774163
AMPLICON |
16S
|
-
|
China
31.14 N 118.37 E |
-
|
|
SRR25774164
AMPLICON |
16S
|
-
|
China
31.14 N 118.36 E |
-
|
|
SRR25774165
AMPLICON |
16S
|
-
|
China
31.14 N 118.35 E |
-
|
|
SRR25774166
AMPLICON |
16S
|
-
|
China
31.14 N 118.34 E |
-
|
|
SRR25774167
AMPLICON |
16S
|
-
|
China
31.14 N 118.141 E |
-
|
|
SRR25774168
AMPLICON |
16S
|
-
|
China
31.14 N 118.140 E |
-
|
|
SRR25774169
AMPLICON |
16S
|
-
|
China
31.14 N 118.139 E |
-
|
|
SRR25774170
AMPLICON |
16S
|
-
|
China
31.14 N 118.138 E |
-
|
|
SRR25774171
AMPLICON |
16S
|
-
|
China
31.14 N 118.137 E |
-
|
|
SRR25774172
AMPLICON |
16S
|
-
|
China
31.14 N 118.136 E |
-
|
|
SRR25774173
AMPLICON |
16S
|
-
|
China
31.14 N 118.135 E |
-
|
|
SRR25774174
AMPLICON |
16S
|
-
|
China
31.14 N 118.134 E |
-
|
|
SRR25774175
AMPLICON |
16S
|
-
|
China
31.14 N 118.133 E |
-
|
|
SRR25774176
AMPLICON |
16S
|
-
|
China
31.14 N 118.132 E |
-
|
|
SRR25774177
AMPLICON |
16S
|
-
|
China
31.14 N 118.33 E |
-
|
|
SRR25774178
AMPLICON |
16S
|
-
|
China
31.14 N 118.131 E |
-
|
|
SRR25774179
AMPLICON |
16S
|
-
|
China
31.14 N 118.130 E |
-
|
|
SRR25774180
AMPLICON |
16S
|
-
|
China
31.14 N 118.129 E |
-
|
|
SRR25774181
AMPLICON |
16S
|
-
|
China
31.14 N 118.128 E |
-
|
|
SRR25774182
AMPLICON |
16S
|
-
|
China
31.14 N 118.127 E |
-
|
|
SRR25774183
AMPLICON |
16S
|
-
|
China
31.14 N 118.126 E |
-
|
|
SRR25774184
AMPLICON |
16S
|
-
|
China
31.14 N 118.125 E |
-
|
|
SRR25774185
AMPLICON |
16S
|
-
|
China
31.14 N 118.124 E |
-
|
|
SRR25774186
AMPLICON |
16S
|
-
|
China
31.14 N 118.123 E |
-
|
|
SRR25774187
AMPLICON |
16S
|
-
|
China
31.14 N 118.122 E |
-
|
|
SRR25774188
AMPLICON |
16S
|
-
|
China
31.14 N 118.32 E |
-
|
|
SRR25774189
AMPLICON |
16S
|
-
|
China
31.14 N 118.23 E |
-
|
|
SRR25774190
AMPLICON |
16S
|
-
|
China
31.14 N 118.22 E |
-
|
|
SRR27936600
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936599
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936591
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936592
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936601
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936553
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936552
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936602
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936555
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936589
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936590
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936593
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936595
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936596
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936597
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27936598
AMPLICON |
16S
|
-
|
Switzerland
46.398830 N 6.232938 E |
-
|
|
SRR27416715
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416551
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416583
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416582
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416581
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416580
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416552
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416729
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416728
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416727
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416724
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416723
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416722
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416721
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416720
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416719
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416550
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416549
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416548
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416718
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416717
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416716
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416556
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416555
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416554
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416730
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416579
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416563
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416562
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416561
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416560
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416559
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416558
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416557
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR21986878
AMPLICON |
16S
|
-
|
USA
42.46 N 98.64 W |
insect microbiome
secretion microbiome |
|
SRR21986879
AMPLICON |
16S
|
-
|
USA
42.46 N 98.64 W |
insect microbiome
secretion microbiome |
|
SRR21986884
AMPLICON |
16S
|
-
|
USA
42.46 N 98.64 W |
insect microbiome
secretion microbiome |
|
SRR21986885
AMPLICON |
16S
|
-
|
USA
42.46 N 98.64 W |
insect microbiome
secretion microbiome |
|
SRR13441157
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441169
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441168
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441167
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441166
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441165
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441163
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441162
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441160
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441159
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441158
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441156
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441155
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441154
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441153
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441152
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441151
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441150
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441149
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441148
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441147
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441145
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441144
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441143
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441141
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441140
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441139
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441132
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441131
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441130
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441129
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR13441128
AMPLICON |
16S
|
-
|
Canada
49.81 N 97.13 W |
ENVO:01000219
laboratory insect colonies |
|
SRR21986882
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986883
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986886
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986870
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986869
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986868
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986871
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986872
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986873
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986874
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986875
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986876
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986877
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986880
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR21986881
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR18464283
AMPLICON |
16S
|
-
|
Russia
56.037048 N 35.500086 E |
Mixed forest [ENVO:01000198]
intestine microbiota |
|
SRR21986887
AMPLICON |
16S
|
-
|
USA
35.74 N 95.15 W |
insect microbiome
secretion microbiome |
|
SRR16095214
AMPLICON |
16S,MLST,wsp,COI,etc.
|
-
|
Australia
|
-
|
|
SRR16763535
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763536
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763537
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763532
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763531
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763530
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763529
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763528
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763527
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763526
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR16763534
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR28812764
AMPLICON |
16S
|
-
|
Japan
43.023083 N 141.416590 E |
-
|
|
SRR28812765
AMPLICON |
16S
|
-
|
Japan
43.023083 N 141.416590 E |
-
|
|
SRR16763533
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR15419898
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Bacteria in the artificial diet
Bacteria in the artificial diet |
|
SRR15419899
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Bacteria in the artificial diet
Bacteria in the artificial diet |
|
SRR15419890
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Bacteria in the artificial diet
Bacteria in the artificial diet |
|
SRR15419891
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Bacteria in the artificial diet
Bacteria in the artificial diet |
|
SRR15419892
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Endosymbiotic bacteria of Paederus fuscipes
Endosymbionts |
|
SRR15419893
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Endosymbiotic bacteria of Paederus fuscipes
Endosymbionts |
|
SRR15419894
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Endosymbiotic bacteria of Paederus fuscipes
Endosymbionts |
|
SRR15419895
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Endosymbiotic bacteria of Paederus fuscipes
Endosymbionts |
|
SRR15419896
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Endosymbiotic bacteria of Paederus fuscipes
Endosymbionts |
|
SRR15419897
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Endosymbiotic bacteria of Paederus fuscipes
Endosymbionts |
|
SRR15419900
AMPLICON |
16S
|
-
|
China
30.81 N 106.06 E |
Endosymbiotic bacteria of Paederus fuscipes
Endosymbionts |
|
SRR19449869
AMPLICON |
16S
|
-
|
China
43.72 N 125.09 E |
-
|
|
SRR19449867
AMPLICON |
16S
|
-
|
China
43.72 N 125.09 E |
-
|
|
SRR19449868
AMPLICON |
16S
|
-
|
China
43.72 N 125.09 E |
-
|
|
SRR19449870
AMPLICON |
16S
|
-
|
China
43.72 N 125.09 E |
-
|
|
SRR19449882
AMPLICON |
16S
|
-
|
China
46.67 N 125.23 E |
-
|
|
SRR19449883
AMPLICON |
16S
|
-
|
China
46.67 N 125.23 E |
-
|
|
SRR19449880
AMPLICON |
16S
|
-
|
China
46.67 N 125.23 E |
-
|
|
SRR19449881
AMPLICON |
16S
|
-
|
China
46.67 N 125.23 E |
-
|
|
SRR19449878
AMPLICON |
16S
|
-
|
China
45.59 N 126.44 E |
-
|
|
SRR19449876
AMPLICON |
16S
|
-
|
China
45.59 N 126.44 E |
-
|
|
SRR19449879
AMPLICON |
16S
|
-
|
China
45.59 N 126.44 E |
-
|
|
SRR19449877
AMPLICON |
16S
|
-
|
China
45.59 N 126.44 E |
-
|
|
SRR19449860
AMPLICON |
16S
|
-
|
China
25.85 N 103.75 E |
-
|
|
SRR19449861
AMPLICON |
16S
|
-
|
China
25.85 N 103.75 E |
-
|
|
SRR19449859
AMPLICON |
16S
|
-
|
China
25.85 N 103.75 E |
-
|
|
SRR19449858
AMPLICON |
16S
|
-
|
China
25.85 N 103.75 E |
-
|
|
SRR15068727
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068726
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068725
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068722
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068723
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068724
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068702
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068703
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068708
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068704
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068705
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068706
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068707
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068729
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068728
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068698
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068699
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068700
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068709
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068710
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068711
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068712
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068713
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068714
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068715
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068716
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068717
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068718
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068701
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068719
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068720
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR15068721
AMPLICON |
16S
|
-
|
China
|
-
|
|
SRR26640740
AMPLICON |
16S
|
-
|
USA
|
ENVO:01000197
Forests |
|
SRR26640739
AMPLICON |
16S
|
-
|
USA
|
ENVO:01000197
Forests |
|
SRR19449874
AMPLICON |
16S
|
-
|
China
28.8 N 112.36 E |
-
|
|
SRR19449873
AMPLICON |
16S
|
-
|
China
28.8 N 112.36 E |
-
|
|
SRR19449871
AMPLICON |
16S
|
-
|
China
28.8 N 112.36 E |
-
|
|
SRR19449872
AMPLICON |
16S
|
-
|
China
28.8 N 112.36 E |
-
|
|
SRR19449866
AMPLICON |
16S
|
-
|
China
35.97 N 116.97 E |
-
|
|
SRR19449865
AMPLICON |
16S
|
-
|
China
35.97 N 116.97 E |
-
|
|
SRR19449862
AMPLICON |
16S
|
-
|
China
35.97 N 116.97 E |
-
|
|
SRR19449863
AMPLICON |
16S
|
-
|
China
35.97 N 116.97 E |
-
|
|
SRR19449857
AMPLICON |
16S
|
-
|
China
31.806 N 116.519 E |
-
|
|
SRR19449864
AMPLICON |
16S
|
-
|
China
31.67 N 116.357 E |
-
|
|
SRR19449854
AMPLICON |
16S
|
-
|
China
31.806 N 116.519 E |
-
|
|
SRR19449855
AMPLICON |
16S
|
-
|
China
31.806 N 116.519 E |
-
|
|
SRR19449856
AMPLICON |
16S
|
-
|
China
31.806 N 116.519 E |
-
|
|
SRR19449852
AMPLICON |
16S
|
-
|
China
31.70 N 116.358 E |
-
|
|
SRR19449853
AMPLICON |
16S
|
-
|
China
31.70 N 116.358 E |
-
|
|
SRR19449875
AMPLICON |
16S
|
-
|
China
31.67 N 116.357 E |
-
|
|
SRR19449884
AMPLICON |
16S
|
-
|
China
31.70 N 116.358 E |
-
|
|
SRR19449885
AMPLICON |
16S
|
-
|
China
31.70 N 116.358 E |
-
|
|
SRR19449886
AMPLICON |
16S
|
-
|
China
31.67 N 116.357 E |
-
|
|
SRR19449887
AMPLICON |
16S
|
-
|
China
31.67 N 116.357 E |
-
|
|
SRR17247056
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247054
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247052
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247051
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247050
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247049
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247048
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247047
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247046
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247045
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247043
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247044
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247066
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247065
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247064
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247063
AMPLICON |
16S
|
-
|
Poland
51.14 N 22.29 E |
-
|
|
SRR17247062
AMPLICON |
16S
|
-
|
Poland
51.14 N 22.29 E |
-
|
|
SRR17247061
AMPLICON |
16S
|
-
|
Poland
51.14 N 22.29 E |
-
|
|
SRR17247060
AMPLICON |
16S
|
-
|
Poland
51.14 N 22.29 E |
-
|
|
SRR17247059
AMPLICON |
16S
|
-
|
Poland
51.14 N 22.29 E |
-
|
|
SRR17247058
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247057
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247055
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247053
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247070
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247069
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247068
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR17247067
AMPLICON |
16S
|
-
|
Poland
51.23 N 22.29 E |
-
|
|
SRR28812766
AMPLICON |
16S
|
-
|
Belgium
50.026488 N 4.622770 E |
-
|
|
SRR28812762
AMPLICON |
16S
|
-
|
Belgium
50.026488 N 4.622770 E |
-
|
|
SRR28812761
AMPLICON |
16S
|
-
|
Belgium
50.026488 N 4.622770 E |
-
|
|
SRR28812760
AMPLICON |
16S
|
-
|
Belgium
50.026488 N 4.622770 E |
-
|
|
SRR28812759
AMPLICON |
16S
|
-
|
Finland
61.55867 N 29.57779 E |
-
|
|
SRR28812758
AMPLICON |
16S
|
-
|
Germany
51.347199 N 7.523855 E |
-
|
|
SRR28812757
AMPLICON |
16S
|
-
|
Germany
50.922011 N 11.585965 E |
-
|
|
SRR28812756
AMPLICON |
16S
|
-
|
Germany
50.922011 N 11.585965 E |
-
|
|
SRR28812768
AMPLICON |
16S
|
-
|
Belgium
50.026488 N 4.622770 E |
-
|
|
SRR28812767
AMPLICON |
16S
|
-
|
Belgium
50.026488 N 4.622770 E |
-
|
|
SRR28812769
AMPLICON |
16S
|
-
|
Germany
49.993330 N 8.243941 E |
-
|
|
SRR10992574
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992562
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992563
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992579
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992578
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992577
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992564
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992576
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992575
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992573
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992572
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992571
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992570
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992569
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992565
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992566
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992567
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR10992568
AMPLICON |
16S
|
-
|
Mexico
19.5312 N 96.9159 W |
-
|
|
SRR12557370
AMPLICON |
24S
|
-
|
China
27.53 N 119.21 E |
Artificial breeding
artifical conditions |
|
SRR11607996
AMPLICON |
16S
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect microbiome
Scolytinae |
|
SRR11607995
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607994
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607993
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607992
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607991
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607990
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11788145
AMPLICON |
ITS
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788144
AMPLICON |
ITS
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788143
AMPLICON |
ITS
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788142
AMPLICON |
ITS
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788141
AMPLICON |
ITS
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect mycobiome
Scolytinae |
|
SRR11607989
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11788140
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11607988
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607987
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607986
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607985
AMPLICON |
16S
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect microbiome
Scolytinae |
|
SRR11607984
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607983
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607982
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11788139
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788138
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788147
AMPLICON |
ITS
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788137
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788136
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788135
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788134
AMPLICON |
ITS
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788133
AMPLICON |
ITS
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect mycobiome
Scolytinae |
|
SRR11607981
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11788132
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788131
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788130
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788129
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11607980
AMPLICON |
16S
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect microbiome
Scolytinae |
|
SRR11607979
AMPLICON |
16S
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect microbiome
Scolytinae |
|
SRR11607978
AMPLICON |
16S
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect microbiome
Scolytinae |
|
SRR11607977
AMPLICON |
16S
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect microbiome
Scolytinae |
|
SRR11607976
AMPLICON |
16S
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect microbiome
Scolytinae |
|
SRR11607975
AMPLICON |
16S
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect microbiome
Scolytinae |
|
SRR11607974
AMPLICON |
16S
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect microbiome
Scolytinae |
|
SRR11607973
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607972
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607971
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607970
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607969
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607968
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607967
AMPLICON |
16S
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect microbiome
Scolytinae |
|
SRR11607966
AMPLICON |
16S
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect microbiome
Scolytinae |
|
SRR11607965
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607964
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607963
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11607962
AMPLICON |
16S
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect microbiome
Scolytinae |
|
SRR11788146
AMPLICON |
ITS
|
-
|
Czech Republic
50.120 N 15.438 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788164
AMPLICON |
ITS
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788163
AMPLICON |
ITS
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788162
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788161
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788160
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788159
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788158
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788157
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788156
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788155
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788154
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788153
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788152
AMPLICON |
ITS
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788151
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788150
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11788149
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR11607997
AMPLICON |
16S
|
-
|
Czech Republic
49.713 N 18.045 E |
Forest insect microbiome
Scolytinae |
|
SRR11788148
AMPLICON |
ITS
|
-
|
Czech Republic
49.173 N 16.317 E |
Forest insect mycobiome
Scolytinae |
|
SRR13754544
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754571
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754570
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754569
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754568
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754567
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754566
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754565
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754554
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754553
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754552
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754550
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754549
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754548
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754547
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754546
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754545
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754543
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754542
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754541
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754539
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754538
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754537
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754536
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754535
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754534
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754533
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754532
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754531
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754530
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754528
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754527
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754526
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754485
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754472
AMPLICON |
16S
|
-
|
USA
36.7022 N 118.9325 W |
-
|
|
SRR13754574
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754573
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754572
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754564
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754563
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754555
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754556
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754557
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754558
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754559
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754560
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754561
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754492
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754491
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754490
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754489
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754488
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754487
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754493
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754494
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754495
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754577
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754576
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754486
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754484
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754483
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754482
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754481
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754480
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754479
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754478
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754477
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754476
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754475
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754575
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR13754471
AMPLICON |
16S
|
-
|
USA
31.72 N 110.88 W |
-
|
|
SRR28812771
AMPLICON |
16S
|
-
|
Germany
49.993330 N 8.243941 E |
-
|
|
SRR28812770
AMPLICON |
16S
|
-
|
Germany
49.993330 N 8.243941 E |
-
|
|
SRR28812763
AMPLICON |
16S
|
-
|
Germany
49.993330 N 8.243941 E |
-
|
|
SRR28812772
AMPLICON |
16S
|
-
|
Germany
49.993330 N 8.243941 E |
-
|
|
SRR12656175
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656174
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656173
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656177
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656176
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656068
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656073
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656072
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656070
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656069
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656067
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656066
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656065
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656064
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656081
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656080
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656079
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656078
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656077
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656076
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656075
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656071
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656082
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656086
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656083
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656087
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656088
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656084
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656123
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656125
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656126
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656127
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656128
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656130
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656131
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656132
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656133
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656134
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656135
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656136
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656090
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656091
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656092
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656093
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656094
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656095
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656097
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656098
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656099
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656100
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656101
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656102
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656103
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656104
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656105
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656106
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656108
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656109
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656110
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656111
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656112
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656113
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656114
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656115
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656116
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656117
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656119
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656120
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656121
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656122
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656124
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656089
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656166
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656167
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656168
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656169
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656170
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656172
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656161
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656162
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656163
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656164
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR12656165
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR8858431
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR8858427
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR8858426
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR8858425
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR8858424
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR8858423
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR8858429
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR8858430
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR8858428
AMPLICON |
16S
|
-
|
Cameroon
7.3276501 N 13.5847197 E |
-
|
|
SRR12656264
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656265
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656256
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656257
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656258
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656259
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656261
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656262
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656255
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR12656263
AMPLICON |
16S
|
-
|
uncalculated
missing |
-
|
|
SRR6131288
AMPLICON |
FLX
|
-
|
New Zealand
43.39 S 172.29 E |
-
|
|
SRR3926754
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926751
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926750
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926749
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926748
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926747
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926746
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926745
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926744
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926743
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926742
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926741
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926740
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926739
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926752
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR3926753
AMPLICON |
16S
|
-
|
China
30.4801 N 114.3645 E |
-
|
|
SRR5753140
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753129
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753138
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753139
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753133
AMPLICON |
16S
|
-
|
Belgium
|
-
|
|
SRR5753132
AMPLICON |
16S
|
-
|
Belgium
|
-
|
|
SRR14748826
AMPLICON |
16S
|
-
|
USA
43.3380 N 89.3804 W |
environmental system
environmental system determined by an organism |
|
SRR5753117
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753118
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753137
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753136
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753130
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753131
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753115
AMPLICON |
16S
|
-
|
Belgium
|
-
|
|
SRR5753116
AMPLICON |
16S
|
-
|
Belgium
|
-
|
|
SRR5753135
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753134
AMPLICON |
16S
|
-
|
Netherlands
|
-
|
|
SRR5753109
AMPLICON |
16S
|
-
|
Belgium
|
-
|
|
SRR5753110
AMPLICON |
16S
|
-
|
Belgium
|
-
|
|
SRR3723141
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723126
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723124
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723127
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723128
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723129
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723130
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723131
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723132
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723133
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723134
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723135
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723136
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723137
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723138
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723139
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723140
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723123
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR3723125
AMPLICON |
16S
|
-
|
USA
40.8148 N 77.8653 W |
-
|
|
SRR2410862
AMPLICON |
16S
|
-
|
Japan
not applicable |
-
|
|
SRR2420890
AMPLICON |
16S
|
-
|
Portugal
not applicable |
-
|
|
SRR5874816
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR5874815
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR5874814
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR5874818
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR5874819
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR5874820
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR5874821
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR5874813
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR5874817
AMPLICON |
16S
|
-
|
USA
38.9637 N 84.0808 W |
-
|
|
SRR27416692
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416691
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416690
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416741
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416740
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416737
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416726
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416725
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416714
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416713
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416712
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416711
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416710
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416709
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416708
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416707
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416706
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416705
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416704
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416703
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416702
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416701
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416700
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416699
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416698
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416697
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416696
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416695
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416694
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416542
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416553
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416564
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416575
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416600
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416618
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416620
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416621
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416622
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416623
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416624
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416625
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416629
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416640
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416643
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416654
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416665
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416683
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416684
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416685
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416686
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416687
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416688
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416689
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416633
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416634
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416635
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416636
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416637
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416638
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416639
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416681
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416641
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416642
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416682
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416739
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416565
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416566
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416567
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416568
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416569
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416570
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416571
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416572
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416573
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416671
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416672
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416673
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416674
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416675
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416676
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416677
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416678
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416679
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416680
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416630
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416631
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|
|
SRR27416632
AMPLICON |
16S
|
-
|
Germany
50.907861 N 11.658028 E |
-
|