R-universe search: topic:copy-number

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bioc

PureCN:Copy number calling and SNV classification using targeted short read sequencing

This package estimates tumor purity, copy number, and loss of heterozygosity (LOH), and classifies single nucleotide variants (SNVs) by somatic status and clonality. PureCN is designed for targeted short read sequencing data, integrates well with standard somatic variant detection and copy number pipelines, and has support for tumor samples without matching normal samples.

Maintained by Markus Riester. Last updated 2 days ago.

copynumbervariation software sequencing variantannotation variantdetection coverage immunooncology bioconductor-package cell-free-dna copy-number loh tumor-heterogeneity tumor-mutational-burden tumor-purity

132 stars 9.88 score 40 scripts

henrikbengtsson

aroma.affymetrix:Analysis of Large Affymetrix Microarray Data Sets

A cross-platform R framework that facilitates processing of any number of Affymetrix microarray samples regardless of computer system. The only parameter that limits the number of chips that can be processed is the amount of available disk space. The Aroma Framework has successfully been used in studies to process tens of thousands of arrays. This package has actively been used since 2006.

Maintained by Henrik Bengtsson. Last updated 1 years ago.

infrastructure proprietaryplatforms exonarray microarray onechannel gui dataimport datarepresentation preprocessing qualitycontrol visualization reportwriting acgh copynumbervariants differentialexpression geneexpression snp transcription affymetrix analysis copy-number dna expression hpc large-scale notebook reproducibility rna

10 stars 5.79 score 112 scripts 3 dependents