Heya,
I've just tried out tophat on all of my QC'd RNAseq data using the the transcriptome as the index, but unfortunately its become snagged!
"Error: segment-based junction search failed with err = -9"
Can anyone offer any solutions? I'd really appreciate it! Thanks,
Craig
(Please excuse the formatting)
$ tophat -o /home/sbica1/tophat/tophatoutput/trinity -r 50 -m 2 -p 8 /home/sbica1/tophat/L.rubellus_trinitytranscriptomeindex/L.rubellus_trinitytranscriptomeindex trimmedop010_1.fastq,trimmedop008_1.fastq,trimmedop009_1.fastq,trimmedop008_3.fastq,trimmedop009_3.fastq trimmedop010_2.fastq,trimmedop008_2.fastq,trimmedop009_2.fastq,trimmedop008_4.fastq,trimmedop009_4.fastq
[Wed Nov 9 19:57:34 2011] Beginning TopHat run (v1.0.14)
-----------------------------------------------
[Wed Nov 9 19:57:34 2011] Preparing output location /home/sbica1/tophat/tophatoutput/trinity/
[Wed Nov 9 19:57:34 2011] Checking for Bowtie index files
[Wed Nov 9 19:57:34 2011] Checking for reference FASTA file
[Wed Nov 9 19:57:34 2011] Checking for Bowtie Bowtie version: 0.12.5.0
[Wed Nov 9 19:57:34 2011] Checking reads seed length: 20bp format: fastq quality scale: phred33 (default)
[Wed Nov 9 22:21:17 2011] Mapping reads against L.rubellus_trinitytranscriptomeindex > with Bowtie
[Wed Nov 9 23:51:38 2011] Joining segment hits
[Thu Nov 10 00:37:24 2011] Mapping reads against L.rubellus_trinitytranscriptomeindex > with Bowtie
[Thu Nov 10 01:56:43 2011] Joining segment hits
[Thu Nov 10 02:37:40 2011] Searching for junctions via segment mapping
[FAILED] Error: segment-based junction search failed with err = -9
Awesome, I'll give this a pop in the morning. Thank you!