Description
A free software tool for Copy Number Variation (CNV) detection from SNP genotyping arrays. Currently it can handle signal intensity data from Illumina and Affymetrix arrays. With appropriate preparation of file format, it can also handle other types of SNP arrays and oligonucleotide arrays.
Home page
https://penncnv.openbioinformatics.org/
Documentation
http://penncnv.openbioinformatics.org/en/latest/user-guide/startup/
License
Free software license.
Usage
Use
module avail PennCNV
to see which versions of PennCNV are available. Use
module load PennCNV/version
to get access to PennCNV.
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