don't use bullets - they are hard to read
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cookbook.md
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cookbook.md
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@ -16,40 +16,40 @@ curl -L https://github.com/lh3/minimap2/releases/download/v2.0/cookbook-data.tgz
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## <a name="map-reads"></a>Mapping Genomic Reads
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* Map example E. coli PacBio reads (takes about 12 wall-clock seconds):
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```sh
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minimap2 -ax map-pb -t4 ecoli_ref.fa ecoli_p6_25x_canu.fa > mapped.sam
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```
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Alternatively, you can create a minimap2 index first and then map:
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```sh
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minimap2 -x map-pb -d ecoli-pb.mmi ecoli_ref.fa # create an index
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minimap2 -ax map-pb ecoli-pb.mmi ecoli_p6_25x_canu.fa > mapped.sam
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```
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This will save you a couple of minutes when you map against the human genome.
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**HOWEVER**, key algorithm parameters such as the k-mer length and window
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size can't be changed after indexing. Minimap2 will give you a warning if
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parameters used in a pre-built index doesn't match parameters on the command
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line. *Please always make sure you are using an intended pre-built index.*
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### Map PacBio reads
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```sh
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minimap2 -ax map-pb -t4 ecoli_ref.fa ecoli_p6_25x_canu.fa > mapped.sam
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```
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Alternatively, you can create a minimap2 index first and then map:
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```sh
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minimap2 -x map-pb -d ecoli-pb.mmi ecoli_ref.fa # create an index
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minimap2 -ax map-pb ecoli-pb.mmi ecoli_p6_25x_canu.fa > mapped.sam
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```
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This will save you a couple of minutes when you map against the human genome.
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**HOWEVER**, key algorithm parameters such as the k-mer length and window
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size can't be changed after indexing. Minimap2 will give you a warning if
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parameters used in a pre-built index doesn't match parameters on the command
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line. *Please always make sure you are using an intended pre-built index.*
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* Map Illumina paired-end reads:
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```sh
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minimap2 -ax sr ecoli_ref.fa ecoli_mason_1.fq ecoli_mason_2.fq > mapped-sr.sam
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```
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### Map Illumina paired-end reads:
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```sh
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minimap2 -ax sr ecoli_ref.fa ecoli_mason_1.fq ecoli_mason_2.fq > mapped-sr.sam
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```
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* Evaluating mapping accuracy with simulated reads:
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```sh
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minimap2 -ax sr ecoli_ref.fa ecoli_mason_1.fq ecoli_mason_2.fq | paftools.js mapeval -
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```
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The output is:
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```
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Q 60 19712 0 0.000000000 19712
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Q 0 282 219 0.010953286 19994
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U 6
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```
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where a line starting with `Q` gives:
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1. Mapping quality (mapQ) threshold
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2. Number of mapped reads between this threshold and the previous mapQ threshold.
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3. Number of wrong mappings in the same mapQ interval
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4. Accumulative mapping error rate
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5. Accumulative number of mappings
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A `U` line gives the number of unmapped reads (for SAM input only)
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### Evaluating mapping accuracy with simulated reads:
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```sh
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minimap2 -ax sr ecoli_ref.fa ecoli_mason_1.fq ecoli_mason_2.fq | paftools.js mapeval -
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```
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The output is:
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```
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Q 60 19712 0 0.000000000 19712
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Q 0 282 219 0.010953286 19994
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U 6
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```
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where a line starting with `Q` gives:
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1. Mapping quality (mapQ) threshold
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2. Number of mapped reads between this threshold and the previous mapQ threshold.
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3. Number of wrong mappings in the same mapQ interval
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4. Accumulative mapping error rate
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5. Accumulative number of mappings
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A `U` line gives the number of unmapped reads (for SAM input only).
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