Comments (1)
Hi Mauro,
for a quicker response, please post your questions at the STAR google group
(https://groups.google.com/forum/?fromgroups=#!forum/rna-star).
The 2-pass scheme is not automated at the moment. I have attached a simple
script with an example of a 2-pass run.
You would need to run the 1st pass with usual parameters, than use the
SJ.out.tab as a splice junction database file to generate a new genome index
for STAR, and then run the 2nd pass of STAR with the new genome index. You can
also add annotated junctions to the 1st and 2nd passes.
If you have many samples, you can collect all the novel junctions from all the
samples (SJ.out.tab files), possibly filter them for reliability, and create
one common set of novel junctions for all samples by merging them. Then you
generate a new genome using annotated junctions and the common set of novel
junctions, and re-run all the samples with this new genome - this would be the
2-nd pass.
Original comment by [email protected]
on 6 Jul 2013 at 3:14
- Added labels: Type-Enhancement
- Removed labels: Type-Defect
Attachments:
from rna-star.
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