GenomicAlignments (version 1.8.4)

Representation and manipulation of short genomic alignments

Description

Provides efficient containers for storing and manipulating short genomic alignments (typically obtained by aligning short reads to a reference genome). This includes read counting, computing the coverage, junction detection, and working with the nucleotide content of the alignments.

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Version

1.8.4

License

Artistic-2.0

Last Published

January 1st, 1970

Functions in GenomicAlignments (1.8.4)