clarify CLR when necessary
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@ -12,7 +12,7 @@ cd minimap2 && make
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./minimap2 -x map-ont -d MT-human-ont.mmi test/MT-human.fa
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./minimap2 -a MT-human-ont.mmi test/MT-orang.fa > test.sam
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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 genomic reads
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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
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./minimap2 -ax sr ref.fa read1.fa read2.fa > aln.sam # short genomic paired-end reads
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@ -139,13 +139,13 @@ parameters at the same time. The default setting is the same as `map-ont`.
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#### <a name="map-long-genomic"></a>Map long noisy genomic reads
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```sh
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minimap2 -ax map-pb ref.fa pacbio-reads.fq > aln.sam # for PacBio subreads
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minimap2 -ax map-pb ref.fa pacbio-reads.fq > aln.sam # for PacBio CLR reads
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minimap2 -ax map-ont ref.fa ont-reads.fq > aln.sam # for Oxford Nanopore reads
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```
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The difference between `map-pb` and `map-ont` is that `map-pb` uses
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homopolymer-compressed (HPC) minimizers as seeds, while `map-ont` uses ordinary
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minimizers as seeds. Emperical evaluation suggests HPC minimizers improve
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performance and sensitivity when aligning PacBio reads, but hurt when aligning
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performance and sensitivity when aligning PacBio CLR reads, but hurt when aligning
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Nanopore reads.
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#### <a name="map-long-splice"></a>Map long mRNA/cDNA reads
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@ -206,7 +206,7 @@ strand field. In this case, each line indicates an oriented junction.
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#### <a name="long-overlap"></a>Find overlaps between long reads
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```sh
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minimap2 -x ava-pb reads.fq reads.fq > ovlp.paf # PacBio read overlap
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minimap2 -x ava-pb reads.fq reads.fq > ovlp.paf # PacBio CLR read overlap
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minimap2 -x ava-ont reads.fq reads.fq > ovlp.paf # Oxford Nanopore read overlap
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```
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Similarly, `ava-pb` uses HPC minimizers while `ava-ont` uses ordinary
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