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Hi
I am a novice in RNA-seq. I am using Sammate to
generate alignment report (read distribution report) from RNA-seq data
that was aligned with Tophat. However, the report shows that 0% of the
reads mapped to junctions and intergenic region. I have never gotten
such results in the past when I was analysing other sets of data. I
think there might be something wrong with the alignment. When viewing
the bam files in IGV, I do see reads that span junctions. I would really
appreciate if you could help me with this.
Thanks
P
Tin Chi Nguyen
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Jan 9, 2013, 1:49:30 PM1/9/13
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Hi,
Can you provide more details on parameters used in SAMMate? I can debug it if you also provide the data you run on.