SD-Genomics / DeviCNV

Detection and Visualization of Exon-Level Copy Number Variants in Targeted Next Generation Sequencing Data

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DeviCNV

Detection and Visualization of Exon-Level Copy Number Variants in Targeted Next Generation Sequencing Data

Environment

DeviCNV runs on Python 2.7 and R 3.2.0.

Python dependencies

  • sys
  • intervaltree
  • intervaltree_bio
  • numpy
  • operator
  • random
  • pysam
  • pyvcf
  • scipy

R dependencies

  • ggplot2
  • PSCBS

Installation

To install DeviCNV, simply download 9 scripts in “Code” directory.

Documentation

PDF documentation is included in the package.

  • DeviCNV1.5 Manual20171101.pdf

Version description

We uploaded DeviCNV_v1.5.1 in 26/06/2019 We fixed some bugs in code.

  1. Delete codes for running with Slurm Workload Manager in "DeviCNV_Example.runningScript.sh"
  2. Fix codes for selecting large segments in "python.scoreCNV.py"

About

Detection and Visualization of Exon-Level Copy Number Variants in Targeted Next Generation Sequencing Data

License:GNU General Public License v3.0


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