
Hello Zohra, For command line (not Galaxy) use of this tool, questions would be best directed to the tool authors at tophat.cufflinks@gmail.com. That said, there appears to be a mismatch between the quality scores in your fastq file and what was expected (integer, linked to the -C option). Should you decide to use Galaxy at http://usegalaxy.org, there are tools to format the input and run this type of job. To help you get started, please see our tutorial covering this exact type of analysis: http://wiki.g2.bx.psu.edu/Learn/Screencasts see "Examples of other analyses -> SOLiD Single End" Hopefully one of these options will work out for you, Best, Jen Galaxy team On 10/11/11 7:47 AM, zohra saci wrote:
Hello, I was trying to run tophat v1.3.2 on SOLID data and I have this error: *zohra@bart:~/Bureau/cancer$ tophat -o /tmp/tophat_SRR036752/ -g 1 -p 4 -C /home/zohra/indexes_bowtie/humain_ SRR036752.fastq
[Tue Oct 11 13:23:53 2011] Beginning TopHat run (v1.3.2) ----------------------------------------------- [Tue Oct 11 13:23:53 2011] Preparing output location /tmp/tophat_SRR036752// [Tue Oct 11 13:23:53 2011] Checking for Bowtie index files [Tue Oct 11 13:23:53 2011] Checking for reference FASTA file [Tue Oct 11 13:23:53 2011] Checking for Bowtie Bowtie version: 0.12.7.0 [Tue Oct 11 13:23:53 2011] Checking for Samtools Samtools Version: 0.1.18 [Tue Oct 11 13:23:53 2011] Generating SAM header for /home/zohra/indexes_bowtie/humain_ [Tue Oct 11 13:23:55 2011] Preparing reads format: fastq quality scale: phred33 (default) [FAILED] Error running 'prep_reads' Error: qual length (51) differs from seq length (51) for fastq record ! * Can you help me. Thanks Zohra Saci
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