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GenomicAlignments

Representation and manipulation of short genomic alignments

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.

Functions (21)

GenomicAlignments

Representation and manipulation of short genomic alignments

v1.26.0
Artistic-2.0
Authors
Hervé Pagès, Valerie Obenchain, Martin Morgan
Initial release

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