===> Please use "Reply All" when responding to this email! <=== Hi Tao, I made an error in my prior reply, it is possible to guide assembly in TopHat. To do this, on the TopHat form, change "TopHat settings to use:" from "Use Defaults" to "Full parameter list". In the expanded form: 1 - change "Use Own Junctions:" to be "yes". 2 - change "Use Gene Annotation Model:" to be "yes" 3 - in the new pull-down menu, select the GTF file from your history Great question! Glad that we were able to provide you with the correct instruction, Best, Jen Galaxy team On 9/15/11 1:38 PM, Jennifer Jackson wrote:
===> Please use "Reply All" when responding to this email! <===
Hello Tao,
Sorry for the delayed reply, your question did not post to the mailing list since the "to" was not _only_ to galaxy-user.
Going forward, please leave off any "to" or "cc" to team members when asking a question. Send all questions directly "to" "galaxy-user@bx.psu.edu" and do not include any "Re" or "Fwd" text in the subject line.
Regarding RNA-seq analysis and reference GTF files, the place to incorporate the GTF file is in the Cufflinks step, the option to select the GTF file from your history is on the tool's form. If you have questions about the tools that are not addressed by these help links:
http://usegalaxy.org/u/jeremy/p/transcriptome-analysis-faq http://usegalaxy.org/u/jeremy/p/galaxy-rna-seq-analysis-exercise
then contacting the tool authors would be the next step: email tophat.cufflinks@gmail.com
To visualize the data, the available options will be links associated with each dataset (expand the dataset box to locate these). The Galaxy Track Browser (GTB) aka "Trackster", UCSC Genome Browser, Ensembl, and GeneTrack are potential options; the datatype will determine which links are provided.
Hopefully this helps,
Best,
Jen Galaxy team
-------- Original Message -------- Subject: run tophat in galaxy Date: Sun, 28 Aug 2011 08:50:04 -0700 From: Peng, Tao <tpeng@fhcrc.org> To: Jennifer Jackson <jen@bx.psu.edu>, galaxy-user <galaxy-user@lists.bx.psu.edu>
Hi how can I specify a GTF gene annotation file when running tophat to guide the alignment to human genome? What is the best way to visualize the tophat results in the context of annotated human genome, i.e. RefSeq?
Thanks,
tao
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