Question: Trouble With Rnaseq Analysis
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gravatar for Cristian Rojas
6.9 years ago by
Cristian Rojas70 wrote:
Hi everybody, I am trying to analyze the differential expression between two RNAseq samples. But I found many troubles aligning my reads. I will describe what I did. First I groomed the FastQ files (2). Then I uploaded the Sorghum genome and aligned the reads to it with Tophat. Aftter that, I tried to use Cufflink with the BAM file of Tophat, using as annotation file an uploaded GTF file and the Sorghum genome, but I received an error message in the three outputs of Cufflink. I tried to align against new brand Maize genome (now at Galaxy), and the same messages. I also converted the BAM file to SAM, but the same. Any advice? What was wrong? Thanks in advance. Cristian
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ADD COMMENTlink modified 6.9 years ago by Jeremy Goecks2.2k • written 6.9 years ago by Cristian Rojas70
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gravatar for Jeremy Goecks
6.9 years ago by
Jeremy Goecks2.2k
Jeremy Goecks2.2k wrote:
Cristian, Please share your history with me (History Options --> Share/Publish --> Share with User --> my email) and I'll take a look. Thanks, J.
ADD COMMENTlink written 6.9 years ago by Jeremy Goecks2.2k
0
gravatar for Jeremy Goecks
6.9 years ago by
Jeremy Goecks2.2k
Jeremy Goecks2.2k wrote:
Cristian, The contig names in your GTF file don't match those in your reference (fasta) file. In order for Cufflinks to use a reference GTF, its contigs names must match those in your reference genome. Best, J.
ADD COMMENTlink written 6.9 years ago by Jeremy Goecks2.2k
0
gravatar for Jeremy Goecks
6.9 years ago by
Jeremy Goecks2.2k
Jeremy Goecks2.2k wrote:
Cristian, The ">" is a formatting character; what needs to match is the string after the ">" in the genome file and the entries in the contig column of your GTF. Your GTF is quite different that your genome file; your genome file has 10 contigs labeled by number, but your GTF has many, many contig names labelled by numbers and names. For Cufflinks to work, you can either (a) turn off bias correction or (b) restrict entries in your GTF to those that match your reference genome. Finally, please reply all to emails so that all emails remain on list for archival and community purposes. Thanks, J.
ADD COMMENTlink written 6.9 years ago by Jeremy Goecks2.2k
Hi Jeremy, I turned off the bias correction and didnt use the genome option, just put the refernde (GTF file), but still the problem. Any help? De: Jeremy Goecks <jeremy.goecks@emory.edu> Para: Cristian Rojas <cristianrojasbr@yahoo.com.ar> CC: galaxy-user@lists.bx.psu.edu Enviado: miércoles, 30 de marzo, 2011 14:25:00 Asunto: Re: [galaxy-user] Trouble with RNAseq analysis Cristian, The ">" is a formatting character; what needs to match is the string after the ">" in the genome file and the entries in the contig column of your GTF. Your GTF is quite different that your genome file; your genome file has 10 contigs labeled by number, but your GTF has many, many contig names labelled by numbers and names. For Cufflinks to work, you can either (a) turn off bias correction or (b) restrict entries in your GTF to those that match your reference genome. Finally, please reply all to emails so that all emails remain on list for archival and community purposes. Thanks, J.
ADD REPLYlink written 6.9 years ago by Cristian Rojas70
I was able to run Cufflinks successfully with bias correction turned off; see the history that I've shared with you. Please try one more time and, if it doesn't work, report it using the bug icon next to the broken dataset. Thanks, J.
ADD REPLYlink written 6.9 years ago by Jeremy Goecks2.2k
I tried agaian and the same problem. I tuned off the bias correction but mantained the GFT file. May be this is the problem? I didnt find your history. Thanks De: Jeremy Goecks <jeremy.goecks@emory.edu> Para: Cristian Rojas <cristianrojasbr@yahoo.com.ar> CC: galaxy-user@lists.bx.psu.edu Enviado: miércoles, 30 de marzo, 2011 16:16:14 Asunto: Re: [galaxy-user] Trouble with RNAseq analysis I was able to run Cufflinks successfully with bias correction turned off; see the history that I've shared with you. Please try one more time and, if it doesn't work, report it using the bug icon next to the broken dataset. Thanks, J.
ADD REPLYlink written 6.9 years ago by Cristian Rojas70
Look for the history I've shared in History Options --> Histories Shared with Me. As requested, if you're still having problems, please report the problematic dataset by clicking on the bug icon. Thanks, J.
ADD REPLYlink written 6.9 years ago by Jeremy Goecks2.2k
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