Re: [galaxy-user] modified "merge" tool
by Iris Vargas Jentzsch
Hello,
I had an issue with the "merge tool some time ago and I sent a message to
this board on the 20th of November last year. I got a reply linking me to
the explanation of the new operations, which I found awesome! Especially for
the Cluster tool :)
I did reply to that message, but it seems like it did not come through. In
that mail I wrote the following:
---
If the Merge tool should output only three columns then there might be
something wrong with it because it actually replaces all the columns that
are not start, end and chromosome with dots instead of eliminating them,
resulting in files with different numbers of columns.
On the other hand, the concatenate tool does combine datasets that have the
same columns in different orders. But if there are additional columns beside
of start, end and chromosome (like the dot columns in the results from the
merge tool), then it gives me an error:
An error occurred running this job: Traceback (most recent call last): File
"./tools/new_operations/gops_concat.py", line 69, in ? main() File
"./tools/new_operations/gops_concat.py", line 62, in main for line in
concat([g1, g2], sameformat=sameformat): File "build/bdist.linux
Here I can’t see the whole error message, so I don’t know if this is useful.
---
The "merge" tool actually continues adding those funny dots for the
additional columns, which I then need to eliminated to continue performing
operations on the file. Therefore I would ask you please to have a look at
it and maybe give the user the choice as to how many columns are needed in
the output (i.e. 1-conserve number of columns or 2-reduce to three columns).
Thanks again,
Iris
======================================
Iris M. Vargas Jentzsch
School of Biological Sciences
University of Canterbury
Private Bag 4800
Christchurch - New Zealand
phone: +64 (0) 3 364 2987 ext 7048
----- Original Message -----
From: "Anton Nekrutenko" <anton(a)bx.psu.edu>
To: "Iris Vargas Jentzsch" <imj15(a)student.canterbury.ac.nz>
Cc: <galaxy-dev(a)bx.psu.edu>
Sent: Wednesday, November 22, 2006 3:01 AM
Subject: Re: [galaxy-user] modified "merge" tool
Iris:
The merge tool still gives you three columns as before. The
concatenate tool now fills absent fields with dots. Here is a
detailed description of new operations:
http://www.bx.psu.edu/cgi-bin/trac.cgi/wiki/GopsDesc
You can use new operation from command line. For this you will need
to download Galaxy and look at how commands are formed within tool
configuration files. Let us know if you need any help with that.
anton
Anton Nekrutenko
Assistant Professor
Department of Biochemistry and Molecular Biology
Center for Comparative Genomics and Bioinformatics
505 Wartik Building
PennState University
University Park, PA 16802
814 865-4752
814 863-6699 FAX
anton(a)bx.psu.edu
http://www.bx.psu.edu/~anton
http://g2.bx.psu.edu
On Nov 19, 2006, at 8:46 PM, Iris Vargas Jentzsch wrote:
> Dear Galaxy team,
>
> I just realized that the “merge” tool in the ‘Operate on Genomic
> intervals” section has been modified (for both the test and the main
> sites). When I used it before, it gave me only three columns as output
> (start, end and chromosome) regardless of the number of columns present
> in the original file. That was actually very handy for me, because it
> meant that after merging output files from different programs
> individually, I could join those into one without problem because the
> columns ended up being the same in all files. Now the tool conserves the
> column number by adding dot columns to reproduce the original number of
> columns. I wonder if there is the possibility to leave this as an option,
> so that the user can choose among conserving number of columns or getting
> a simplified version with only three output columns like before. I know
> I can simply cut the columns I want out to another file, but it is an
> additional step, and when processing a lot of files, if the connection is
> slow or the server is busy it takes ages :(
>
> Otherwise I would be very happy if someone can tell me how to use galaxy
> directly from the command line… That would make my life so much easier :)
>
> Thank you,
>
> Iris
>
>
>
> ======================================
> Iris M. Vargas Jentzsch
> School of Biological Sciences
> University of Canterbury
> Private Bag 4800
> Christchurch - New Zealand
> phone: +64 (0) 3 364 2987 ext 7048
> _______________________________________________
> Galaxy-user mailing list
> Galaxy-user(a)bx.psu.edu
> http://mail.bx.psu.edu/cgi-bin/mailman/listinfo/galaxy-user
13 years, 8 months
error with EMBOSS tools
by Ross Hardison
Using Galaxy test I tried to run three different ORF-finders from
EMBOSS: "getorf", "sixpack" and "transeq". All of them gave the same
error:
"An error occurred running this job: sixpack: error while loading
shared libraries: libX11.so.6: cannot open shared object file: No
such file or directory"
Ross Hardison
T. Ming Chu Professor of Biochemistry and Molecular Biology
The Pennsylvania State University
304 Wartik Laboratory
University Park, PA 16802
e-mail: rch8(a)psu.edu
phone: 814-863-0113 FAX: 814-863-7024
13 years, 8 months
(no subject)
by E Bouhassira
I am trying to use the gencode partition software but when I tried to
access the lnked with the documentation I get a login windows to login to
genome.imem.es
Is this software restricted to some users?
How can I get access?
--
Using Opera's revolutionary e-mail client: http://www.opera.com/mail/
13 years, 8 months
