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caution that the splice:sr is experimental
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@@ -21,7 +21,7 @@ cd minimap2 && make
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./minimap2 -ax splice -uf -k14 ref.fa reads.fa > aln.sam # noisy Nanopore direct RNA-seq
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./minimap2 -ax splice:hq -uf ref.fa query.fa > aln.sam # PacBio Kinnex/Iso-seq (RNA-seq)
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./minimap2 -ax splice --junc-bed anno.bed12 ref.fa query.fa > aln.sam # use annotated junctions
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./minimap2 -ax splice:sr ref.fa r1.fq r2.fq > aln.sam # short-read RNA-seq (r1236 or later)
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./minimap2 -ax splice:sr ref.fa r1.fq r2.fq > aln.sam # short-read RNA-seq (r1236+; experimental)
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./minimap2 -cx asm5 asm1.fa asm2.fa > aln.paf # intra-species asm-to-asm alignment
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./minimap2 -x ava-pb reads.fa reads.fa > overlaps.paf # PacBio read overlap
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./minimap2 -x ava-ont reads.fa reads.fa > overlaps.paf # Nanopore read overlap
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@@ -40,7 +40,7 @@ man ./minimap2.1
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- [Map long mRNA/cDNA reads](#map-long-splice)
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- [Find overlaps between long reads](#long-overlap)
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- [Map short genomic reads](#short-genomic)
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- [Map short RNA-seq reads](#short-rna-seq)
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- [Map short RNA-seq reads (experimental & evolving)](#short-rna-seq)
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- [Full genome/assembly alignment](#full-genome)
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- [Advanced features](#advanced)
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- [Working with >65535 CIGAR operations](#long-cigar)
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@@ -231,14 +231,16 @@ be paired if they are adjacent in the input stream and have the same name (with
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the `/[0-9]` suffix trimmed if present). Single- and paired-end reads can be
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mixed.
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#### <a name="short-rna-seq"></a>Map short RNA-seq reads
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#### <a name="short-rna-seq"></a>Map short RNA-seq reads (experimental & evolving)
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```sh
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minimap2 -ax splice:sr ref.fa reads-se.fq > aln.sam # single-end
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minimap2 -ax splice:sr ref.fa r1.fq r2.fq > aln.sam # paired-end
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```
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The new preset `splice:sr` was added between v2.28 and v2.29. It functions
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similarly to `sr` except that it performs spliced alignment.
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similarly to `sr` except that it performs spliced alignment. Note that this
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functionality is ***experiemental*** and evolving. It is better not to use it
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for production.
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#### <a name="full-genome"></a>Full genome/assembly alignment
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