CNVkit Genome-wide copy number from targeted DNA sequencing CNVkit 0.8.1 documentation

Copy number calling pipeline. Text and tabular reports. Compatibility and other IO. Calling copy number gains and losses. Whole-genome sequencing and targeted amplicon capture. Python API cnvlib package. CNVkit Genome-wide copy number from targeted DNA sequencing. CNVkit Genome-wide copy number from targeted DNA sequencing. Apache License 2.0. Download the reference genome. Map sequencing reads to the reference genome. Build a reference from normal samples and infer tumor copy ratios. FAQ and How To.

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TITLE

CNVkit Genome-wide copy number from targeted DNA sequencing CNVkit 0.8.1 documentation

DESCRIPTION

Copy number calling pipeline. Text and tabular reports. Compatibility and other IO. Calling copy number gains and losses. Whole-genome sequencing and targeted amplicon capture. Python API cnvlib package. CNVkit Genome-wide copy number from targeted DNA sequencing. CNVkit Genome-wide copy number from targeted DNA sequencing. Apache License 2.0. Download the reference genome. Map sequencing reads to the reference genome. Build a reference from normal samples and infer tumor copy ratios. FAQ and How To.

CONTENT

This web site had the following in the homepage, "Calling copy number gains and losses." Our analyzers noticed that the web page stated " Whole-genome sequencing and targeted amplicon capture." The Website also said " CNVkit Genome-wide copy number from targeted DNA sequencing. CNVkit Genome-wide copy number from targeted DNA sequencing. Map sequencing reads to the reference genome. Build a reference from normal samples and infer tumor copy ratios."

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