EnsembleCNV: an ensemble machine learning algorithm to identify and genotype copy number variation using SNP array data

The associations between diseases/traits and copy number variants (CNVs) have not been systematically investigated in genome-wide association studies (GWASs), primarily due to a lack of robust and accurate tools for CNV genotyping. Herein, we propose a novel ensemble learning framework, ensembleCNV,...

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Bibliografiske detaljer
Udgivet i:Nucleic Acids Res
Main Authors: Zhang, Zhongyang, Cheng, Haoxiang, Hong, Xiumei, Di Narzo, Antonio F, Franzen, Oscar, Peng, Shouneng, Ruusalepp, Arno, Kovacic, Jason C, Bjorkegren, Johan L M, Wang, Xiaobin, Hao, Ke
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2019
Fag:
Methods Online
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6468244/
https://ncbi.nlm.nih.gov/pubmed/30722045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkz068
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