@@ -14,13 +14,13 @@ cd minimap2 && make
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# use presets (no test data)
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./minimap2 -ax map-pb ref.fa pacbio.fq.gz > aln.sam # PacBio CLR genomic reads
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./minimap2 -ax map-ont ref.fa ont.fq.gz > aln.sam # Oxford Nanopore genomic reads
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- ./minimap2 -ax map-hifi ref.fa pacbio-ccs.fq.gz > aln.sam # PacBio HiFi/CCS genomic reads (v2.19 or later )
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- ./minimap2 -ax lr:hq ref.fa ont-Q20.fq.gz > aln.sam # Nanopore Q20 genomic reads (v2.27 or later )
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+ ./minimap2 -ax map-hifi ref.fa pacbio-ccs.fq.gz > aln.sam # PacBio HiFi/CCS genomic reads (v2.19+ )
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+ ./minimap2 -ax lr:hq ref.fa ont-Q20.fq.gz > aln.sam # Nanopore Q20 genomic reads (v2.27+ )
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./minimap2 -ax sr ref.fa read1.fa read2.fa > aln.sam # short genomic paired-end reads
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./minimap2 -ax splice ref.fa rna-reads.fa > aln.sam # spliced long reads (strand unknown)
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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 or traditional cDNA
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- ./minimap2 -ax splice --junc-bed anno.bed12 ref.fa query.fa > aln.sam # prioritize on annotated junctions
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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 -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
@@ -39,7 +39,7 @@ man ./minimap2.1
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- [ Map long noisy genomic reads] ( #map-long-genomic )
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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 accurate genomic reads] ( #short-genomic )
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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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- [ Full genome/assembly alignment] ( #full-genome )
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- [ Advanced features] ( #advanced )
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