Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • axiom7
    Member
    • Aug 2009
    • 14

    #1

    Problem running cb_local; maybe manifest file?

    Hi,
    I am trying to run crossbow against a local fastq file that I have. I downloaded the hg18.jar file and I believe everything (or most everything) is configured correctly.

    The command I execute is:

    smwilson@axiom7:~/disk/crossbow-1.1.2$ ./cb_local --reference crossbow_refs/hg18 --input crossbow_refs/hg18/GTCA.manifest --output crossbow_refs/hg18/output --keep-all --cpus 4 --bowtie-args "-n2 -l28 -e 70 --trim5 4"

    Contents of the manifest file is shown below, and the file exists:

    smwilson@axiom7:~/disk/crossbow-1.1.2$ cat crossbow_refs/hg18/GTCA.manifest
    /disk/smwilson/BerwickData_NCGR/input/GTCA.fastq
    smwilson@axiom7:~/disk/crossbow-1.1.2$ ls -l /disk/smwilson/BerwickData_NCGR/input/GTCA.fastq

    -rwxr-x--- 1 smwilson smwilson 2520434410 2012-03-08 14:22 /disk/smwilson/BerwickData_NCGR/input/GTCA.fastq

    It seems as if Align.pl does not like my manifest file.

    Thanks.
    Susan

    ******
    * Warning: No TOOLNAME file in tool directory: Bin
    * Align.pl: s3cmd: found: , given:
    * Align.pl: jar: found: /usr/bin/jar, given:
    * Align.pl: hadoop: found: , given:
    * Align.pl: wget: found: /usr/bin/wget, given:
    * Align.pl: s3cfg:
    * Align.pl: bowtie: found: /home/smwilson/disk/bowtie-0.12.7/bowtie, given: /home/smwilson/disk/bowtie-0.12.7/bowtie
    * Align.pl: partition len: 1000000
    * Align.pl: ref:
    * Align.pl: quality: phred33
    * Align.pl: truncate at: 0
    * Align.pl: discard mate: 0
    * Align.pl: discard reads < truncate len: 0
    * Align.pl: SAM passthrough: 0
    * Align.pl: Straight through: 0
    * Align.pl: local index path: /disk/smwilson/crossbow-1.1.2/crossbow_refs/hg18/index/index
    * Align.pl: counters: /home/smwilson/output_counters/counters.txt
    * Align.pl: dest dir:
    * Align.pl: bowtie args: --partition 1000000 --mm -t --hadoopout --startverbose -n2 -l28 -e 70 --trim5 4
    * Align.pl: ls -al
    * Align.pl: total 0
    * drwxr-xr-x 2 smwilson smwilson 100 2012-03-15 13:16 .
    * drwxr-xr-x 3 smwilson smwilson 60 2012-03-15 13:16 ..
    * -rw-r--r-- 1 smwilson smwilson 0 2012-03-15 13:16 .tmp.29756
    * -rw-r--r-- 1 smwilson smwilson 0 2012-03-15 13:16 .tmp.29780
    * -rw-r--r-- 1 smwilson smwilson 0 2012-03-15 13:16 .tmp.29804
    * Align.pl: Retrived 0 counters from previous stages
    * Align.pl: Read first line of stdin:
    * /disk/smwilson/BerwickData_NCGR/input/GTCA.fastq
    * Bad number of read tokens ; expected 3 or 5:
    * /disk/smwilson/BerwickData_NCGR/input/GTCA.fastq
    ******
  • axiom7
    Member
    • Aug 2009
    • 14

    #2
    I take it back. It seems as if Align.pl does not like the fastq file itself.

    Comment

    • narain
      Banned
      • Aug 2011
      • 73

      #3
      Okay, so how do you run crossbow on a local file ? I tried it for .fastq.gz file too and it did not work. Any suggestions if you have sorted it out already ?

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
        by SEQadmin2



        Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

        Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
        ...
        10-14-2026, 09:55 AM
      • SEQadmin2
        New Genomics Technologies Take Aim at Long-Standing Limits
        by SEQadmin2


        Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

        We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
        ...
        09-28-2026, 10:25 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      19 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      26 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-13-2026, 09:56 AM
      0 responses
      22 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-09-2026, 11:14 AM
      0 responses
      28 views
      0 reactions
      Last Post SEQadmin2  
      Working...