Subread Sequence Alignment and Counting for R
DescriptionAlignment, quantification and analysis of second and third generation sequencing data. Includes functionality for read mapping, read counting, SNP calling, structural variant detection and gene fusion discovery. Can be applied to all major sequencing techologies and to both short and long sequence reads.
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Install this software package
If the package is available for the distribution you are currently using on your computer then install the software by clicking on…Install r-bioc-rsubread