It allows for fast reading and processing of genome read and annotation files such as gtf/gff/bed/bam. In addition, it also provides functions for advanced manipulations such as filling missing intron coordinates, extracting non-overlapping intron coordinates, extracting overlapping genes etc.
|Annotation Coverage DataImport RNASeq Sequencing Software
|Arunkumar Srinivasan <email@example.com>
|View on GitHub
Install the latest version of this package by entering the following in R:
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