PGG SNV

PGG SNV compiles human single nucleotide variation (SNV) data and provides population-genetic and molecular-evolutionary analyses, with emphasis on under-studied indigenous populations in Asia to support comparative and evolutionary studies.


Key Features:

  • Extensive Data Archive: Contains 265 million SNVs from 220,147 present-day genomes and 1,018 ancient genomes, including 1,009 newly sequenced genomes representing 977 global populations.
  • Emphasis on Indigenous Asian Populations: Prioritizes inclusion of under-investigated indigenous populations in Asia to enhance representation of global genetic diversity.
  • Population Genetic Diversity and Evolutionary Parameters: Provides estimates of population genetic diversity and various evolutionary parameters for comparative analyses.
  • Heatmap Plot of Population Differentiation: Visualizes genetic differentiation across populations to identify population-specific variation.
  • Word Map Plot of Allele Frequency Distributions: Displays allele frequency distributions across populations to summarize variant prevalence and patterns.
  • Manhattan Plot of Natural Selection Signals: Identifies genomic regions with signals of natural selection across populations.
  • Heatmap Plot for Linkage Disequilibrium Analysis: Visualizes linkage disequilibrium patterns to assess non-random associations between loci.

Scientific Applications:

  • Population Genetics: Enables analysis of allele frequencies, population differentiation, and genetic diversity across contemporary and ancient genomes.
  • Molecular Evolution: Supports detection and interpretation of natural selection signals and evolutionary parameter estimation.
  • Anthropological Genomics: Facilitates comparative studies of human demographic history and population structure, with temporal perspective from ancient genomes.
  • Medical Genetics: Aids investigation of potential links between SNVs and disease susceptibility or resistance across diverse populations.

Methodology:

Computational visualization and analysis methods include heatmap plots for population differentiation and linkage disequilibrium, word map plots for allele frequency distributions, and Manhattan plots for natural selection signals.

Topics

Details

Added:
1/9/2020
Last Updated:
1/9/2021

Operations

Publications

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 B, Xu S. PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations. Genome Biology. 2019;20(1). doi:10.1186/s13059-019-1838-5. PMID:31640808. PMCID:PMC6805450.

PMID: 31640808
PMCID: PMC6805450
Funding: - Strategic Priority Research Program: XDB13040100 - Key Research Program of Frontier Sciences: QYZDJ-SSW-SYS009 - National Natural Science Foundation of China: 31501011, 31711530221, 31771388, 91731303 - National Science Fund for Distinguished Young Scholars: 31525014 - Program of Shanghai Academic Research Leader: 16XD1404700 - National Key Research and Development Program: 2016YFC0906403 - UK Royal Society-Newton Advanced Fellowship: NAF\R1\191094 - Shanghai Municipal Science and Technology Major Project: 2017SHZDZX01 - Chinese Academy of Sciences President’s International Fellowship Initiatives: 2017VBA0008

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