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

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

Abstract Despite the tremendous growth of the DNA sequencing data in the last decade, our understanding of the human genome is still in its infancy. To understand the implications of genetic variants in the light of population genetics and molecular evolution, we developed a database, PGG.SNV (https...

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Bibliographic Details
Main Authors: Chao Zhang, Yang Gao, Zhilin Ning, Yan Lu, Xiaoxi Zhang, Jiaojiao Liu, Bo Xie, Zhe Xue, Xiaoji Wang, Kai Yuan, Xueling Ge, Yuwen Pan, Chang Liu, Lei Tian, Yuchen Wang, Dongsheng Lu, Boon-Peng Hoh, Shuhua Xu
Format: Article
Language:English
Published: BMC 2019-10-01
Series:Genome Biology
Subjects:
Human diversity
Population genetics and genomics
Single nucleotide variations
Indigenous populations
Population prevalence
Variant annotation
Online Access:http://link.springer.com/article/10.1186/s13059-019-1838-5

Internet

http://link.springer.com/article/10.1186/s13059-019-1838-5

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