seqCNA-package: Copy number analysis of deep sequencing cancer data
In seqCNA: Copy number analysis of high-throughput sequencing cancer data
Description
Fast summarization, extensive filtering and improved normalization
Details
Package: seqCNA
Type: Package
Version: 1.13.0
Date: 2014-01-09
License: GPL-3
applyFilters applyThresholds plotCNProfile readSeqsumm runGLAD runSeqnorm runSeqsumm writeCNProfile
Author(s)
David Mosen-Ansorena
Maintainer: David Mosen-Ansorena <dmosen.gn@cicbiogune.es>
seqCNA documentation built on Nov. 8, 2020, 7:09 p.m.
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Description
Fast summarization, extensive filtering and improved normalization
Details
| Package: | seqCNA |
| Type: | Package |
| Version: | 1.13.0 |
| Date: | 2014-01-09 |
| License: | GPL-3 |
applyFilters applyThresholds plotCNProfile readSeqsumm runGLAD runSeqnorm runSeqsumm writeCNProfile
Author(s)
David Mosen-Ansorena
Maintainer: David Mosen-Ansorena <dmosen.gn@cicbiogune.es>
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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