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Hi all,
as you know I started to test the aligners both with simulated and real data.
It comes that the simulation tool is able to generate directly FASTQ files (and
not solexa.txt). So we have two different kind of data: the original generated
from the sequencer (.txt) and the FASTQ.
As you know the vast majority of the modules have been developed starting from
.txt, some of them starting from them starting from the fastq, and the reason
is that some tools have internal routines that do the conversion, others have
not.
BTW, with the sim data I started with BOWTIE SE. As the simulated data are
fastq I have customized my pipeline removing the conversion step and adjusting
the parameters accordingly. The validation is ok, but the process doesn't work
and I have got errors with no streams.
I am also attaching the pipe I modified...am I doing something wrong? It is
important for me as I have to modify many pipes to test those fastq.
Tks,
Fed
Original issue reported on code.google.com by [email protected] on 20 Sep 2011 at 6:22
I looked at your workflow and there doesn't seem to be anything wrong with it.
It runs fine for me on fgene1. Since you are running these on fgene3 and are
getting errors, I suspect it is a server related error but I don't have access
to fgene3 to verify this.
Original issue reported on code.google.com by
[email protected]
on 20 Sep 2011 at 6:22Attachments:
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