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Copy Number Variation Detection Using Total Variation

Next-generation sequencing (NGS) technologies offer new opportunities for precise and accurate identification of genomic aberrations, including copy number variations (CNVs). For high-throughput NGS data, using depth of coverage has become a major approach to identify CNVs, especially for whole exom...

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Bibliografiske detaljer
Udgivet i:ACM BCB
Main Authors: Zare, Fatima, Nabavi, Sheida
Format: Artigo
Sprog:Inglês
Udgivet: 2019
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7278034/
https://ncbi.nlm.nih.gov/pubmed/32515750
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1145/3307339.3342181
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