An accurate and powerful method for copy number variation detection

MOTIVATION: Integration of multiple genetic sources for copy number variation detection (CNV) is a powerful approach to improve the identification of variants associated with complex traits. Although it has been shown that the widely used change point based methods can increase statistical power to...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Bioinformatics
Egile Nagusiak: Xiao, Feifei, Luo, Xizhi, Hao, Ning, Niu, Yue S, Xiao, Xiangjun, Cai, Guoshuai, Amos, Christopher I, Zhang, Heping
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2019
Gaiak:
Original Papers
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6735918/
https://ncbi.nlm.nih.gov/pubmed/30649252
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty1041
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