PGG.SNV
Names
More detailed information about this field from each metasource.
PGG.SNV
metasource: Fairsharing.org
version: None
PGG SNV
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
PGG_SNV
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
Names
More detailed information about this field from each metasource.
PGG.SNV
metasource: Fairsharing.orgversion: None
PGG SNV
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
PGG_SNV
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
Names
More detailed information about this field from each metasource.
PGG.SNV
metasource: Fairsharing.orgversion: None
PGG SNV
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
PGG_SNV
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
PGG.SNV is database for understanding the evolutionary and medical implications of human single nucleotide variation (SNV) on a population level. It documents more than 300,000 genomes and 10 billion allele frequencies records for diverse human ethnic groups.
Description
More detailed information about this field from each metasource.
PGG.SNV is database for understanding the evolutionary and medical implications of human single nucleotide variation (SNV) on a population level. It documents more than 300,000 genomes and 10 billion allele frequencies records for diverse human ethnic groups.
metasource: Fairsharing.orgversion: None
PGG SNV is a database for understanding evolutionary and medical implications of human single nucleotide variations in diverse populations. The tool provides useful web tools for figure illustration. Users can upload their local files with specific format (see readme and example at the top-right corner of each tool) generated by their own analysis to draw their figures as well as download them. The current version includes tools on (a) heatmap plot of population differentiation; (b) word map plot of allele frequency distributions; (c) manhattan plot of natural selection signals; and (d) heatmap plot for linkage disequilibrium analysis.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
Webpage:
https://www.pggsnv.orgWebpage
More detailed information about this field from each metasource.
https://www.pggsnv.org
metasource: Fairsharing.orgversion: None
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
Publications:
Publications
More detailed information about this field from each metasource.
PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
PMID: 31640808
metasource: Fairsharing.org
version: None
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
Publications
More detailed information about this field from each metasource.
PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
PMID: 31640808
metasource: Fairsharing.org
version: None
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
PubMed citations: 10.
10 articles citing: PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
Association of Hypoxia-Inducible Factor 1α Gene Polymorphisms With Breast Cancer Susceptibility: A Meta-Analysis. PMID:35507894
Genomic diversity and post-admixture adaptation in the Uyghurs. PMID:35350227
Genetic association of TMPRSS2 rs2070788 polymorphism with COVID-19 case fatality rate among Indian populations. PMID:34995811
Advances in integrative African genomics. PMID:34740451
Regional TMPRSS2 V197M Allele Frequencies Are Correlated with COVID-19 Case Fatality Rates. PMID:34588322
Fine-Scale Genetic Structure and Natural Selection Signatures of Southwestern Hans Inferred From Patterns of Genome-Wide Allele, Haplotype, and Haplogroup Lineages. PMID:34504517
False Alarms in Consumer Genomics Add to Public Fear and Potential Health Care Burden. PMID:33113957
Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations. PMID:32936832
Indigenous Genomic Databases: Pragmatic Considerations and Cultural Contexts. PMID:32391301
Database Resources of the National Genomics Data Center in 2020. PMID:31702008
Tags:
Tags
More detailed information about this field from each metasource.
sequence variant
metasource: Fairsharing.org
version: None
single nucleotide polymorphism
metasource: Fairsharing.org
version: None
mapping
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
population genetics
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
population genomics
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
human biology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
genetic variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:12.310942
Tags
More detailed information about this field from each metasource.
sequence variant
metasource: Fairsharing.orgversion: None
single nucleotide polymorphism
metasource: Fairsharing.orgversion: None
mapping
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
population genetics
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
population genomics
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
human biology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
genetic variation
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:12.310942
sequence variant single nucleotide polymorphism mapping population genetics population genomics human genetic variation
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