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  • thinkRNA
    Member
    • Jan 2010
    • 94

    #1

    Running tophat with unmated pairs

    There seems to be no description of how to run tophat if you are using unpaired sequence reads. Does it only work for mated pairs?

    When I give it my commands, this is the error:
    Error: you must set the mean inner distance between mates with -r

    But, I don't have mates?
  • simonandrews
    Simon Andrews
    • May 2009
    • 870

    #2
    Originally posted by thinkRNA View Post
    There seems to be no description of how to run tophat if you are using unpaired sequence reads. Does it only work for mated pairs?
    No, you can definitely use it for single end sequences. You just supply one sequence file instead of two.

    tophat /path/to/indices fastq_file

    Comment

    • Cole Trapnell
      Senior Member
      • Nov 2008
      • 213

      #3
      As noted in the manual, multiple (single end) FASTQ files can be provided as a comma separated list. When you have paired end reads, you need *two* comma separated lists.

      Comment

      • thinkRNA
        Member
        • Jan 2010
        • 94

        #4
        Thanks, I did get it going. But now, I get this error:

        [Thu Feb 11 09:37:18 2010] Preparing output location ./tophat_out/
        [Thu Feb 11 09:37:18 2010] Checking for Bowtie index files
        [Thu Feb 11 09:37:18 2010] Checking for reference FASTA file
        [Thu Feb 11 09:37:18 2010] Checking for Bowtie
        Bowtie version: 0.11.3.0
        [Thu Feb 11 09:37:18 2010] Checking reads
        seed length: 27bp
        format: fastq
        quality scale: phred33 (default)
        [Thu Feb 11 09:37:18 2010] Mapping reads against mm9 with Bowtie
        [Thu Feb 11 09:37:21 2010] Joining segment hits
        [Thu Feb 11 09:37:21 2010] Searching for junctions via segment mapping
        Warning: junction database is empty!
        [Thu Feb 11 09:38:12 2010] Joining segment hits
        [Thu Feb 11 09:38:13 2010] Reporting output tracks

        Does any one know how to fix this warning? I am using UCSC mm9 and thought the chromosome naming problem should disappear.

        Comment

        • middlemale
          Member
          • Feb 2010
          • 16

          #5
          in my case, single end read and I try to use gene model annotation
          tophat -G <GFF3 file> /path/to/indices fastq_file

          same problem "Error: you must set the mean inner distance between mates with -r"

          and if without -G <GFF3 file> in options, that works fine.

          any suggest of how adding -G option? cheers

          Comment

          • Thomas Doktor
            Senior Member
            • Apr 2009
            • 105

            #6
            middlemale, could you copy-paste the exact command you used to launch TopHat, as you've typed it?

            Comment

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