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Package: r-bioc-rsubread (2.8.1-1)

Subread Sequence Alignment and Counting for R

Alignment, 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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Download for all available architectures
Architecture Package Size Installed Size Files
amd64 7,963.0 kB35101 kB [list of files]
arm64 7,977.2 kB35061 kB [list of files]
ppc64el 8,065.4 kB35473 kB [list of files]