DeviCNV
Detection and Visualization of Exon-Level Copy Number Variants in Targeted Next Generation Sequencing Data
Install / Use
/learn @SD-Genomics/DeviCNVREADME
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.
- Delete codes for running with Slurm Workload Manager in "DeviCNV_Example.runningScript.sh"
- Fix codes for selecting large segments in "python.scoreCNV.py"
