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Thread | Thread Starter | Forum | Replies | Last Post |
how --mate-inner-dist and --mate-std-dev affect the tophat mapping result | liuxq | Bioinformatics | 0 | 11-06-2011 09:53 PM |
always reads on plus strand more than on minus strand | tujchl | Bioinformatics | 4 | 04-29-2011 01:08 AM |
different number of reads mapped to plus strand and minus strand | gfmgfm | Bioinformatics | 2 | 02-03-2011 11:26 AM |
RNA-Seq: Multimodal RNA-seq using single-strand, double-strand, and CircLigase-based | Newsbot! | Literature Watch | 0 | 12-24-2010 03:13 AM |
How does inner distances(--mate-inner-dist and --mate-std-dev) work in tophat? | Gangcai | Bioinformatics | 4 | 06-15-2010 06:53 AM |
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#1 |
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Location: italy Join Date: Sep 2010
Posts: 14
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Hi everybody,
I'm performing downstream pair-end analysis on Genome Analyzer II data. The reads was aligned against a reference genome using BWA that gives a BAM output. I'm a novice and I have to understand some basic topic in order to build my pipeline. For example in the flag field I found 0x0010 (strand of the query) and 0x0020 (strand of the mate); what exactly mean they? I mean, the reads are both given in the forward strand or not? To extract the two sequences readed by GAII, have I to do some transformation (i.e. sense to antisense)?? Thanks! |
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#2 |
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Location: 41°17'49"N / 2°4'42"E Join Date: Oct 2008
Posts: 323
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It means exactly that. That flag in your BAM record tells you what is the orientation that the aligner used to map the read. And since you are in a pair-end experiment, the other flag 0x20 comes into play also. It contains the same information but for the other end of the read.
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-drd |
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flag, strand |
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