Hello Jiwen,
It is possible to view both the TopHat and Cufflinks output together in
Trackster. Are you doing this?
Are you seeing that reads/transcripts are spanning the splice regions
(align to one side, span the gap, then align to the other side)? This is
what would be expected for RNA-seq data.
It might help to import a known transcript track from UCSC or Biomart
and visualize that, to get a better understanding of how genomic
features are represented in the Trackster UI.
If you have an error dataset from an RNA-seq tool, you can send in a bug
report, but that doesn't seem to be the case. Rather, there is a
question about how the calculation are done. For cases like that, the
tool authors might be the best source for help. Contact info is in this
wiki link "Example: unexpected results with RNA-seq analysis tools."
http://wiki.g2.bx.psu.edu/Support#Unexpected_scientific_result
Hopefully this helps,
Best,
Jen
Galaxy team
On 2/3/12 7:24 AM, 杨继文 wrote:
Dear all,
Today I used Tophat to map the reads from RNA-Seq, and had a look at the
results using "visaulization" function. In some regions I can see splice
junctions calculated by Tophat, but I don't see any reads mapping to
this region. Is this a bit strange? I thought "splice junction" is
calculated from the mapped reads.
However, I think cufflinks only uses "accepted hits" as input, maybe it
is not a big problem that "splice junction' is not accurate.
Am I right? Was there something wrong when I mapped my reads with tophat?
Hope you can help me figure it out.
Looking forward to hearing from you.
Jiwen
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