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A Density Peak-Based Method to Detect Copy Number Variations From Next-Generation Sequencing Data

Copy number variation (CNV) is a common type of structural variations in human genome and confers biological meanings to human complex diseases. Detection of CNVs is an important step for a systematic analysis of CNVs in medical research of complex diseases. The recent development of next-generation...

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Detalles Bibliográficos
Autores principales:	Xie, Kun, Tian, Ye, Yuan, Xiguo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838601/ https://www.ncbi.nlm.nih.gov/pubmed/33519925 http://dx.doi.org/10.3389/fgene.2020.632311

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