PennCNV-tumor

Inference of copy number variation/abberation

Brought to you by: gchen98, tumorim

As of 2016-11-29, this project can be found here.

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Last Update: 2016-02-10

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PennCNV-tumor is software that is appropriate for inferring copy number variation or abberations in germline or tumor tissue respectively. It takes in as input data either signal intensity from genotyping microarrays or aligned read counts from shotgun sequencing experiments. The software is written in C++ and targeted for unix/linux platforms.

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2013-06-21

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