CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies

Genome-wide association studies (GWASs) have revolutionized the field of complex trait genetics over the past decade, yet for most of the significant genotype-phenotype associations the true causal variants remain unknown. Identifying and interpreting how causal genetic variants confer disease susce...

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Detalhes bibliográficos
Publicado no:Nucleic Acids Res
Main Authors: Wang, Jianhua, Huang, Dandan, Zhou, Yao, Yao, Hongcheng, Liu, Huanhuan, Zhai, Sinan, Wu, Chengwei, Zheng, Zhanye, Zhao, Ke, Wang, Zhao, Yi, Xianfu, Zhang, Shijie, Liu, Xiaorong, Liu, Zipeng, Chen, Kexin, Yu, Ying, Sham, Pak Chung, Li, Mulin Jun
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2020
Assuntos:
Database Issue
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7145620/
https://ncbi.nlm.nih.gov/pubmed/31691819
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkz1026
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