Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • fongchun
    Member
    • May 2011
    • 55

    TopHat - Segment Join Failed

    Hi,

    I've been searching around the forum for a solution to this problem, but I've haven't found any solutions which have worked for me. I am just trying to run TopHat on a bunch of paired-end read libraries and I keep running into this segment join failed issue.

    [fong@beast fong]$ tophat -r 200 -o /share/lustre/fong/results/ABC_VS_GCB/tophat/HS0637,hg19 hg19 /share/lustre/gascoyne/WTSS/DLBCL/raw_data/HS0637/reads.1.fastq /share/lustre/gascoyne/WTSS/DLBCL/raw_data/HS0637/reads.2.fastq

    [Thu May 12 10:21:34 2011] Beginning TopHat run (v1.2.0)
    -----------------------------------------------
    [Thu May 12 10:21:34 2011] Preparing output location /share/lustre/fong/results/ABC_VS_GCB/tophat/HS0637,hg19/
    [Thu May 12 10:21:35 2011] Checking for Bowtie index files
    [Thu May 12 10:21:35 2011] Checking for reference FASTA file
    [Thu May 12 10:21:35 2011] Checking for Bowtie
    Bowtie version: 0.12.7.0
    [Thu May 12 10:21:35 2011] Checking for Samtools
    Samtools Version: 0.1.11
    [Thu May 12 10:22:43 2011] Checking reads
    min read length: 50bp, max read length: 75bp
    format: fastq
    quality scale: phred33 (default)
    [Thu May 12 11:42:29 2011] Mapping reads against hg19 with Bowtie
    [Thu May 12 11:42:30 2011] Joining segment hits
    [FAILED]
    Error: Segment join failed with err = 1

    I've tried taking a small subset of the reads and it works fine, but when I scale it to use all the reads it returns this error. Can anyone provide any advice on how to fix this problem? Thanks,

    Fong
  • fongchun
    Member
    • May 2011
    • 55

    #2
    If this means anything to anyone, I somehow solved the problem by just changing some of my parameters. I removed the 'comma' in my output dir and then gave the absolute path to the reference index. So the following command I used was:

    tophat -r 200 -o /share/lustre/fong/results/ABC_VS_GCB/tophat/HS0637 /share/lustre/fong/annotation_files/bowtie/indexes/hg19 /share/lustre/gascoyne/WTSS/DLBCL/raw_data/HS0637/reads.1.fastq /share/lustre/gascoyne/WTSS/DLBCL/raw_data/HS0637/reads.2.fastq

    I had the BOWTIE_INDEXES environment variable set to the directory "/share/lustre/fong/annotation_files/bowtie/indexes/" so I theoretically shouldn't need to give it the absolute path. And it should have complained at the mapping set and not the joining segment hits step if it was an index problem. But whatever the case, these two modifications made tophat work.

    Fong

    Comment

    Latest Articles

    Collapse

    • GATTACAT
      Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
      by GATTACAT
      Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
      07-01-2026, 11:43 AM
    • SEQadmin2
      Nine Things a Sample Prep Scientist Thinks About Before Sequencing
      by SEQadmin2


      I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

      Here are nine questions we think about, in roughly the order they matter, before...
      06-18-2026, 07:11 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Yesterday, 11:08 AM
    0 responses
    6 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-30-2026, 05:37 AM
    0 responses
    11 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-26-2026, 11:10 AM
    0 responses
    19 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-17-2026, 06:09 AM
    0 responses
    53 views
    0 reactions
    Last Post SEQadmin2  
    Working...