The CNVRanger package implements a comprehensive tool suite for CNV analysis. This includes functionality for summarizing individual CNV calls across a ...

The CNVRanger package implements a comprehensive tool suite for the analysis of copy number variation (CNV). This includes functionality for summarizing ...

We present the CNVRanger R/Bioconductor package which implements a comprehensive toolbox for structured downstream analysis of CNVs.

The CNVRanger package implements a comprehensive tool suite for CNV analysis. This includes functionality for summarizing individual CNV calls across a ...

1 февр. 2020 г. · We present the CNVRanger R/Bioconductor package which implements a comprehensive toolbox for structured downstream analysis of CNVs.

Introduction. Copy number variation (CNV) is a frequently observed deviation from the diploid state due to duplication or deletion of genomic regions.

Functionality for CNV analysis. Contribute to waldronlab/CNVRanger development by creating an account on GitHub.

The 'CNVRanger' software tool is an R package designed for the structured downstream analysis of copy number variations (CNVs). It offers a comprehensive ...

CNVRanger uses Bioconductor core data structures implemented in the GenomicRanges and RaggedExperiment packages to represent, access, and manipulate CNV data.

Man pages for CNVRanger. Summarization and expression/phenotype association of CNV ranges. cnvEQTL, CNV-expression association analysis. cnvGWAS ...