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CNV-P: a machine-learning framework for predicting high confident copy number variations

BACKGROUND: Copy-number variants (CNVs) have been recognized as one of the major causes of genetic disorders. Reliable detection of CNVs from genome sequencing data has been a strong demand for disease research. However, current software for detecting CNVs has high false-positive rates, which needs...

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Detalles Bibliográficos
Autores principales:	Wang, Taifu, Sun, Jinghua, Zhang, Xiuqing, Wang, Wen-Jing, Zhou, Qing
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	PeerJ Inc. 2021
Materias:	Bioinformatics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645205/ https://www.ncbi.nlm.nih.gov/pubmed/34917425 http://dx.doi.org/10.7717/peerj.12564

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