Description

Copy number variant detection from high-throughput sequencing data

Input

Name
Description
Pattern

0 ()

1 ()

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1 ()

0 ()

1 ()

0 ()

1 ()

0 ()

1 ()

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Output

Name
Description
Pattern

bed ()

cnn ()

cnr ()

cns ()

pdf ()

png ()

versions ()

Tools

cnvkit Documentation

CNVkit is a Python library and command-line software toolkit to infer and visualize copy number from high-throughput DNA sequencing data. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina and Ion Torrent.

License: Apache-2.0
Authors