Update wolf_tutorial
@ -49,15 +49,21 @@ Not working yet...
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### 1. Import the sequencing data in a DMS
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### 1. Import the sequencing data in a DMS
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Download the reads:
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[wolf_F.fastq.gz](/uploads/09dada3587189c3b3a7af7024981c074/wolf_F.fastq.gz)
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[wolf_R.fastq.gz](/uploads/a95dbad14b75474c8307cab56fa083ca/wolf_R.fastq.gz)
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1. Import the first set of reads, with :
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1. Import the first set of reads, with :
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obi import --quality-solexa wolf_tutorial/wolf_F.fastq wolf/reads1
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obi import --quality-solexa wolf_tutorial/wolf_F.fastq.gz wolf/reads1
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`--quality-solexa` is the appropriate fastq quality option because it's an old dataset, `wolf_tutorial/wolf_F.fastq` is the path to the file to import, `wolf` is the path to the DMS that will be automatically created, and `reads1` is the name of the view into which the file will be imported.
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`--quality-solexa` is the appropriate fastq quality option because it's an old dataset, `wolf_tutorial/wolf_F.fastq` is the path to the file to import, `wolf` is the path to the DMS that will be automatically created, and `reads1` is the name of the view into which the file will be imported.
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2. Import the second set of reads:
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2. Import the second set of reads:
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obi import --quality-solexa wolf_tutorial/wolf_R.fastq wolf/reads2
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obi import --quality-solexa wolf_tutorial/wolf_R.fastq.gz wolf/reads2
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3. Import the [ngsfilter file](https://pythonhosted.org/OBITools/scripts/ngsfilter.html) describing the primers and tags used for each sample:
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3. Import the [ngsfilter file](https://pythonhosted.org/OBITools/scripts/ngsfilter.html) describing the primers and tags used for each sample:
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