Calculates the coverage of a set of genomic regions given the fragments generated by sequencing experiments as ChIP-seq, ChIP-exo or ChIP-nexus.
Package details |
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Author | Rene Welch <welch@stat.wisc.edu> |
Bioconductor views | Alignment ChIPSeq Coverage DNASeq DataImport RNASeq Sequencing Transcription Visualization |
Maintainer | Rene Welch <welch@stat.wisc.edu> |
License | GPL (>=2) |
Version | 1.0 |
URL | https:github.com/welch16/Segvis/issues |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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