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...

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Veröffentlicht in:Bioinformatics
Hauptverfasser: Xiao, Feifei, Luo, Xizhi, Hao, Ning, Niu, Yue S, Xiao, Xiangjun, Cai, Guoshuai, Amos, Christopher I, Zhang, Heping
Format: Artigo
Sprache:Inglês
Veröffentlicht: Oxford University Press 2019
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Original Papers
Online Zugang: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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