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Inferring copy number variants in high-coverage human genomes with next-generation sequencing data.
Inferring copy number variants in high-coverage human genomes with next-generation sequencing data.
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Summary
Inferring copy number variants in high-coverage human genomes with next-generation sequencing data.
Last Updated
May 7, 2018 at 11:59
License
Free to academia and non-profit organizations
Total Downloads
5.4K
Supported Platforms