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.
|Bioconductor views||Annotation Coverage DataImport RNASeq Sequencing Software|
|Maintainer||Arunkumar Srinivasan <[email protected]>|
|Package repository||View on GitHub|
Install the latest version of this package by entering the following in R:
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