An exome sequencing pipeline for identifying and genotyping common CNVs associated with disease with application to psoriasis

Motivation: Despite the prevalence of copy number variation (CNV) in the human genome, only a handful of confirmed associations have been reported between common CNVs and complex disease. This may be partially attributed to the difficulty in accurately genotyping CNVs in large cohorts using array-ba...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Coin, Lachlan J.M., Cao, Dandan, Ren, Jingjing, Zuo, Xianbo, Sun, Liangdan, Yang, Sen, Zhang, Xuejun, Cui, Yong, Li, Yingrui, Jin, Xin, Wang, Jun
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2012
Fag:
Original Papers
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3436806/
https://ncbi.nlm.nih.gov/pubmed/22962454
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bts379
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker