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About: CNV calling from NGS data
URL: https://cran.r-project.org/web/packages/saasCNV/; https://zhangz05.u.hpc.mssm.edu/saasCNV/

saasCNV is a package for the analysis of somatic copy number alterations (SCNAs) of tumor samples using WGS, WES and SNP array data.

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Related Medical Scholarly Articles (MedicalScholarlyArticle 1) #

Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data

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