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saasCNV #
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Structured data

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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0.210 Allele-specific copy number profiling by next-generation DNA sequencing
0.051 CODEX
0.050 falcon
0.030 ngCGH
0.025 GWAS
0.025 HDF5
0.025 Targeted DNA sequencing
0.025 Copy-number variation
0.025 September 13
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