openanalytics/gcount: Obtain Raw Read Counts from RNASeq Data
Count reads that fall under a feature (gene, exon or intron) by removing ambiguous and/or overlapping reads for downstream analyses.
Getting started
Browse package contents
Package details |
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| Bioconductor views | DifferentialExpression GeneExpression RNASeq Sequencing Software |
| Maintainer | Arunkumar Srinivasan <asrinivasan@openanalytics.eu> |
| License | GPL-3 |
| Version | 0.99.0 |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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