Did we miss something? Our COVID-19 Collection is growing, but not yet complete. Tell us what's missing. Email contact@fairsharing.org or add missing resources to our spreadsheet

ready PGG.SNV

General Information
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.

Homepage https://www.pggsnv.org

Countries that developed this resource China

Created in 2017

Taxonomic range





Awaiting DOI assignment.

Publication for citation  PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations. Zhang C,Gao Y,Ning Z,Lu Y,Zhang X,Liu J,Xie B,Xue Z,Wang X,Yuan K,Ge X,Pan Y,Liu C,Tian L,Wang Y,Lu D,Hoh BP,Xu S; Genome Biol ; 2019; 10.1186/s13059-019-1838-5;


Record added: March 17, 2020, 2:36 p.m.
Record updated: March 18, 2020, 12:57 p.m. by The FAIRsharing Team.

Show edit history


In Collections

Support

General

Additional Information





Publications

PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Zhang C,Gao Y,Ning Z,Lu Y,Zhang X,Liu J,Xie B,Xue Z,Wang X,Yuan K,Ge X,Pan Y,Liu C,Tian L,Wang Y,Lu D,Hoh BP,Xu S
Genome Biol 2019

View Paper (PubMed) View Publication

Related Standards

Reporting Guidelines

No guidelines defined

Terminology Artifacts

No semantic standards defined

Models and Formats

No syntax standards defined

Identifier Schemas

No identifier schema standards defined

Metrics

No metrics standards defined


Related Databases

Implementing Policies

This record is not implemented by any policy.