RTCGA/RTCGA.cnv: CNV (Copy-number variation) datasets from The Cancer Genome Atlas Project
Package provides CNV (based on Merge snp) datasets from The Cancer Genome Atlas Project for all cohorts types from http://gdac.broadinstitute.org/. Data format is explained here https://wiki.nci.nih.gov/display/TCGA/Retrieving +Data+Using+the+Data+Matrix. Data from 2015-11-01 snapshot.
Getting started
Browse package contents
Package details |
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| Author | Przemyslaw Biecek <przemyslaw.biecek@gmail.com> |
| Bioconductor views | Annotation Data |
| Maintainer | Marcin Kosinski <m.p.kosinski@gmail.com> |
| License | GPL-2 |
| Version | 0.99.4 |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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