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  • Joshua_HIT
    Junior Member
    • Oct 2013
    • 8

    Tophat2 stucked

    Hi:

    I want to run tophat2 on four sets of data(human chimp gibbon gorilla). For human I downloaded hg19 from USCS in which Bowtie2 index has been included, so human has been finished successfully. but for other three spices I have to use "bowtie2-build refgene.fa genome" to build index on my own.

    the problem is: for all index established by me, tophat2 can not run successfully!! It will stucked on process below:


    [2013-12-07 18:26:04] Beginning TopHat run (v2.0.9)
    -----------------------------------------------
    [2013-12-07 18:26:04] Checking for Bowtie
    Bowtie version: 2.1.0.0
    [2013-12-07 18:26:04] Checking for Samtools
    Samtools version: 0.1.19.0
    [2013-12-07 18:26:04] Checking for Bowtie index files (genome)..
    [2013-12-07 18:26:04] Checking for reference FASTA file
    [2013-12-07 18:26:04] Generating SAM header for ../../Bowtie2_Index/Chimp/chimp
    format: fastq
    quality scale: phred33 (default)
    [2013-12-07 18:26:57] Preparing reads
    left reads: min. length=101, max. length=101, 81784737 kept reads (75486 discarded)
    right reads: min. length=101, max. length=101, 81747073 kept reads (113150 discarded)
    [2013-12-07 19:48:52] Mapping left_kept_reads to genome chimp with Bowtie2

    2 hours have passed... and nothing changed. I have not seen any error on any action before...I think the problem are bowtie indexes I build.
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    If you have a large data set then it is not unusual to have the job run for several hours (2 hr is not a lot).

    Have patience. As long as the process is running no need to worry.

    Comment

    • dpryan
      Devon Ryan
      • Jul 2011
      • 3478

      #3
      If you want RNAseq reads aligned more quickly then you need to use something like STAR (though it requires MUCH more RAM).

      Comment

      • Joshua_HIT
        Junior Member
        • Oct 2013
        • 8

        #4
        Originally posted by GenoMax View Post
        If you have a large data set then it is not unusual to have the job run for several hours (2 hr is not a lot).

        Have patience. As long as the process is running no need to worry.

        you are totally right. I am a new freshman on biology, I indeed need more patient! Thanks!!

        Comment

        • Joshua_HIT
          Junior Member
          • Oct 2013
          • 8

          #5
          Originally posted by dpryan View Post
          If you want RNAseq reads aligned more quickly then you need to use something like STAR (though it requires MUCH more RAM).
          Thanks for your advise. I would have a look on that!

          Comment

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