Details
| Name | Canvas |
|---|---|
| Version | |
| Description | Canvas (Copy Number Variant Caller) is a tool for calling copy number variants (CNVs) from human DNA sequencing data. It can work either with germline data, or paired tumor/normal samples. Its primary input is aligned reads (in .bam format), and its primary output is a report (in a .vcf file) giving the copy number status of the genome. |
| Homepage | https://github.com/Illumina/canvas |
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