r-exomedepth
Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.
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Summary
Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.
Last Updated
Jun 30, 2025 at 14:13
License
GPL-3
Total Downloads
25.1K
Supported Platforms
linux-64
macOS-64