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Minimap2 is a versatile sequence alignment program that aligns DNA or mRNA sequences against a large reference database.
19 lines
621 B
Plaintext
19 lines
621 B
Plaintext
Minimap2 is a versatile sequence alignment program that aligns DNA or mRNA
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sequences against a large reference database. Typical use cases include:
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(1) mapping PacBio or Oxford Nanopore genomic reads to the human genome
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(2) finding overlaps between long reads with error rate up to ~15%
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(3) splice-aware alignment of PacBio Iso-Seq or Nanopore cDNA or Direct RNA
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readsagainst a reference genome
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(4) aligning Illumina single- or paired-end reads
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(5) assembly-to-assembly alignment
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(6) full-genome alignment between two closely related species with divergence
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below ~15%
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WWW: https://github.com/lh3/minimap2
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