vastgroup / vast-tools

A toolset for profiling alternative splicing events in RNA-Seq data.
MIT License
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Analysis never ends #42

Closed attakata closed 9 years ago

attakata commented 9 years ago

We are highly interested in your vast-tools. However the analysis always stuck at the point below (we have waited for more than a week).

vast-tools align test/1.fastq test/2.fastq [vast align]: Setting output directory to /mnt/dbs03/home/takata/analysis/vast-tools/vast_out [vast align]: Setting tmp directory.. [vast align]: Set tmp directory to /mnt/dbs03/home/takata/analysis/vast-tools/vast_out/tmp! [vast align]: Trimming fastq sequences to 50 nt sequences [vast trim]: Total processed reads: 2500 [vast trim]: Total valid fwd reads: 2500 [vast trim]: Total valid rev reads: 2500 [vast align]: Doing genome substraction

This was the case even if we reduced the number of reads to 2500 and used multiple 2.4GHz cores.

Required software is seemingly installed successfully as follows.

./install.R Using R version 3.2.1 (2015-06-18) Looking for VAST Database [VASTDB] Found what appears to be VASTDB.. OK Trying to load required package: MASS Trying to load required package: getopt Trying to load required package: optparse Trying to load required package: RColorBrewer Trying to load required package: reshape2 Trying to load required package: ggplot2 Trying to load required package: grid Trying to load required package: parallel Trying to load required package: devtools Loading required package: psiplot Setting vast-tools permissions... success! /usr/bin/bowtie Found bowtie... Everything looks --OK

We appreciate if you could tell us how long it usually take to finish the analysis and/or whether our environment may have some problem.

mirimia commented 9 years ago

This is strange. It seems to be stuck on the first bowtie run. I guess you had run bowtie before without any problems? Does it create the trimmed fasta file normally? Perhaps it could have to do with the namings of the fastq files (but i doubt it). Try just in case to run it with compressed fastq files named "reads1.fq.gz" or so.

Thanks

kcha commented 9 years ago

Hi @attakata, can you also try running the analysis using the supplied test data with VASTDB? The FASTQ files should be located under: <your VASTDB path>/Hsa/FASTQ/

attakata commented 9 years ago

Dear mirmia and kcha, Thanks a lot for your suggestion. Installation of bowtie and setting of PATH looks to have some problem. When I reinstalled it and add the bowtie directory to PATH vast-tools align works successfully.

Best,