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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
Member
Location: CA Join Date: Nov 2008
Posts: 34
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hi, guys, I was wondering what's your take on this. Tophat will accept reads that are mapped up to 20 locations and take a fraction for each location. Well, this could be helpful to identify homologous genes, but also create a lots artifact. Do you think we should stay with reads that mapped only once in the genome?
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#2 |
Senior Member
Location: Stockholm, Sweden Join Date: Feb 2008
Posts: 319
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That's not "monoclonal" reads, but rather "multi-mapping" reads.
Personally I think it is too restrictive to require unique mappings in RNA-seq. It's a matter of taste as well as organism + application. |
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