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



 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

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

Source: https://archive.org/



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