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Using SAAS-CNV to Detect and Characterize Somatic Copy Number Alterations in Cancer Genomes from Next Generation

Zhongyang Zhang1, Ke Hao2

  • 1Department of Genetics and Genomic Sciences, Icahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Methods in Molecular Biology (Clifton, N.J.)
|July 25, 2018
PubMed

Keywords:
Cancer genomeCopy number variationNext-generation sequencingSAAS-CNVSNP arraySegmentationSomatic copy number alterationWhole-exome sequencingWhole-genome sequencing

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