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 Vol 15: Copy number variation detection using next generation sequencing read counts.


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This article is from BMC Bioinformatics, volume 15.AbstractBackground: A copy number variation (CNV) is a difference between genotypes in the number of copies of a genomic region. Next generation sequencing (NGS) technologies provide sensitive and accurate tools for detecting genomic variations that include CNVs. However, statistical approaches for

Autor: Wang, Heng; Nettleton, Dan; Ying, Kai

Fuente: https://archive.org/







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