drramki-chop/edm: Scalable workflow to identify copy Number variants from exome sequencing data
Provides optimized and scalable functions to call copy number variants (CNVs) from exome sequencing data.
Getting started
Browse package contents
Package details |
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| Author | Ramakrishnan Rajagopalan, Shiva Ganesan |
| Maintainer | Ramakrishnan Rajagopalan <rajagopalanr@email.chop.edu> |
| License | GPL-3 |
| Version | 0.0.1 |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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