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  • Mudita
    Member
    • Oct 2012
    • 15

    #1

    Error while running DEXSeq

    I am working with Illumina RNAseq data. My experiment contain 5-5 biological replicates of normal and treated. Initially I followed cufflink-->cuffdiff workflow (Trimmomatics-->Tophat-->Cufflinks-->Cuffmerge-->Cuffdiff), but could not get any significant genes/isoform.

    Later I started working working with HTSeq-->EdgeR workflow (Trimmomatics-->Tophat-->HTSeq-->EdgeR) and could get around 1000 significant genes.

    Now I am looking for isoform information and so I started working DEXSeq package.

    I am getting following error while running dexseq_count.py:

    Traceback (most recent call last):
    File "/data/RNASEQdata/Programs/dexseq_count.py", line 70, in <module>
    for f in HTSeq.GFF_Reader( gff_file ):
    File "/home/gadgil/.local/lib/python2.7/site-packages/HTSeq/__init__.py", line 210, in __iter__
    for line in FileOrSequence.__iter__( self ):
    File "/home/gadgil/.local/lib/python2.7/site-packages/HTSeq/__init__.py", line 51, in __iter__
    lines = open( self.fos )
    IOError: [Errno 2] No such file or directory: '-'

    These are the steps I have followed:

    python dexseq_prepare_annotation.py Homo_sapiens.GRCh37.71.gtf DEXSeq.gtf

    samtools view accepted_hits.bam | python /dexseq_count.py -p no -s no -a 10 - DEXSeq.gtf output/19_N.txt

    Please help me with this error.

    Thanks in advance.

    Best Regards,
    Mudita
  • areyes
    Senior Member
    • Aug 2010
    • 165

    #2
    Hi @Mudita,

    Have a look at the pasilla vignette, it contains examples of how to use the python scripts of the DEXSeq package: first you would have to convert the bam file into sam, sort it by read name and then run the python scripts.

    Alternatively, have a look at the section "9.3 From GRanges, BamListFiles and transcriptDb objects" will indicate you how to generate an ExonCountSet object within R directly from bam files.

    Alejandro

    Comment

    • Mudita
      Member
      • Oct 2012
      • 15

      #3
      Thanks for your reply

      However, my bam file is already sorted by read name. Same kind of input i have already given to htseq and it worked there. The only difference of input I could see from HTSeq to DEXSeq, is the preperation of annotations file.

      I downloaded annotation gtf file from ensemble:
      http://asia.ensembl.org/info/data/ftp/index.html

      I did this:
      python dexseq_prepare_annotation.py Homo_sapiens.GRCh37.71.gtf DEXSeq.gtf

      Comment

      • areyes
        Senior Member
        • Aug 2010
        • 165

        #4
        Hi @Mudita,

        Sorry for my previous post (that I already deleted), it was incorrect!

        I think the problem is the order of the parameters try this:

        samtools view accepted_hits.bam | python /dexseq_count.py -p no -s no -a 10 DEXSeq.gtf - output/19_N.txt
        Last edited by areyes; 04-18-2013, 03:08 AM.

        Comment

        • Mudita
          Member
          • Oct 2012
          • 15

          #5
          Thank you very much

          it is working now. But it was just the matter of hyphen (-) before output file. I would have never figure it out.
          Thanks again.

          I would like to ask one more question here.
          DEXSeq would only find out differentially expressed exons. However, I am also interested in splice junctions, which tool you would recommend other than cuffdiff.

          Mudita

          Comment

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