ExomeDepth

Calls Copy Number Variants from Targeted Sequence Data

CRAN Package

Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.

  • Version1.1.15
  • R version≥ 3.4.0
  • LicenseGPL-3
  • Needs compilation?Yes
  • Last release01/09/2020

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  • Depends1 package
  • Imports10 packages
  • Suggests1 package