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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Database Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145620/
https://www.ncbi.nlm.nih.gov/pubmed/31691819
http://dx.doi.org/10.1093/nar/gkz1026

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145620/
https://www.ncbi.nlm.nih.gov/pubmed/31691819
http://dx.doi.org/10.1093/nar/gkz1026

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