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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Genome Biol
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2019
Gaiak:
Database
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6805450/
https://ncbi.nlm.nih.gov/pubmed/31640808
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-019-1838-5
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak