Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans

De novo mutations (DNMs) significantly contribute to sporadic diseases, particularly in neuropsychiatric disorders. Whole-exome sequencing (WES) and whole-genome sequencing (WGS) provide effective methods for detecting DNMs and prioritizing candidate genes. However, it remains a challenge for scient...

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Detalles Bibliográficos
Autores principales: Zhao, Guihu, Li, Kuokuo, Li, Bin, Wang, Zheng, Fang, Zhenghuan, Wang, Xiaomeng, Zhang, Yi, Luo, Tengfei, Zhou, Qiao, Wang, Lin, Xie, Yali, Wang, Yijing, Chen, Qian, Xia, Lu, Tang, Yu, Tang, Beisha, Xia, Kun, Li, Jinchen
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/PMC7145562/
https://www.ncbi.nlm.nih.gov/pubmed/31642496
http://dx.doi.org/10.1093/nar/gkz923

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