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

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://www.pg...

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Detalles Bibliográficos
Autores principales: Zhang, Chao, Gao, Yang, Ning, Zhilin, Lu, Yan, Zhang, Xiaoxi, Liu, Jiaojiao, Xie, Bo, Xue, Zhe, Wang, Xiaoji, Yuan, Kai, Ge, Xueling, Pan, Yuwen, Liu, Chang, Tian, Lei, Wang, Yuchen, Lu, Dongsheng, Hoh, Boon-Peng, Xu, Shuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Database
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805450/
https://www.ncbi.nlm.nih.gov/pubmed/31640808
http://dx.doi.org/10.1186/s13059-019-1838-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805450/
https://www.ncbi.nlm.nih.gov/pubmed/31640808
http://dx.doi.org/10.1186/s13059-019-1838-5

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