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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
Member
Location: il Join Date: Jun 2010
Posts: 64
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Hi everyone,
I am using bwa to align Illumina reads. I used the -r option in order to specify the read group. In the output sam file I am getting read groups only for the aligned reads. Reads that are not mapped (with '*' in the chromosome and position) don't have a read group. In the downstream analysis I use GATK, which gives errors because of this. Any suggestions how to overcome this? Thanks |
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#2 |
Junior Member
Location: Nottingham, UK Join Date: Nov 2009
Posts: 8
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I have the same problem, I also use bwa -r for alignment.
When I re-run TableRecalibrate with the added parameter --default_read_group name_of_my_read_group it seems to work and ignores the unmapped reads. However, I'm not sure this will cause any trouble in downstream analysis? |
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#3 |
Senior Member
Location: Boston Join Date: Feb 2008
Posts: 693
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