Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • sp_wade
    Junior Member
    • Mar 2010
    • 9

    #1

    HELP, about HPeak

    Hi! I `m trying to do a peak detection using HPeak2.1.

    I run the command line as following:

    perl HPeak.pl -format BED -t treatment_tags.bed -c control.bed -n FoxA1

    But there seems to be something wrong,the program reports a message:
    "
    Wed Jul 21 19:07:37 2010
    ##### process raw data in treated sample and get summary.
    No such file or directory
    Application Error: child process (summary.pl) exited abnormally.
    "
    However, the treatment_tags.bed and control.bed are do in the work space!
    Who can tell me what `s wrong,and what should I do?
    Thanks!
    Last edited by sp_wade; 07-21-2010, 04:26 AM.
  • sp_wade
    Junior Member
    • Mar 2010
    • 9

    #2
    HI! I downloaded a 2.0 version and found a sample.
    It used a media file "*.inp" to locate the treatment and control file.
    So I created a media file and successfully solved the problem!
    Thanks!

    Comment

    • Bioinfo
      Member
      • Jul 2010
      • 15

      #3
      Hi
      I am new to ChipSeq. shall i ask you some questins regarding Hpeak? you may think is very easy however i am a newbie.
      Even I have the got same error message which you had. did u tried with windows or else you tried with linux only? if so which versions of Hpeak and Illumina Pipeline. and how could we know the experiment name used (FoxA1).
      thanks
      Last edited by Bioinfo; 07-29-2010, 01:35 AM.

      Comment

      • sp_wade
        Junior Member
        • Mar 2010
        • 9

        #4
        HI!Bioinfo!
        I tried with linux. you may try a 2.0 version first from http://www.sph.umich.edu/csg/qin/HPeak/Download.html ,and do as the manual, In the 2.0 package,there is an example folder in which includes "chip.inp" and "mock.inp". Open the .inp file ,you will find the filename of the control data or ChIP data.
        you can run a command line just like this:
        perl HPeak.pl -format BED -t chip.inp -c mock.inp -n sample
        the format BED must be adjusted to the format of the input data, while the experiment name all depends on you!

        Good luck!

        Originally posted by Bioinfo View Post
        Hi
        I am new to ChipSeq. shall i ask you some questins regarding Hpeak? you may think is very easy however i am a newbie.
        Even I have the got same error message which you had. did u tried with windows or else you tried with linux only? if so which versions of Hpeak and Illumina Pipeline. and how could we know the experiment name used (FoxA1).
        thanks

        Comment

        • Husen
          Junior Member
          • Nov 2010
          • 7

          #5
          You need to create a media/temp/text (or any file) and store path of your input data file as it's content, so content of the text file (let's name it treat.txt) may look like this:
          /home/xyz/path-of-datafile/test_data.bed

          to run Hpeak:
          perl HPeak.pl -format BED -t treat.txt

          Also consider, BED format which is required by HPeak is different from the one used by UCSC Genome browser (refer to the manual).

          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, 10-22-2026, 11:13 AM
          0 responses
          23 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-22-2026, 10:48 AM
          0 responses
          20 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-15-2026, 10:52 AM
          0 responses
          36 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-14-2026, 05:39 AM
          0 responses
          42 views
          0 reactions
          Last Post SEQadmin2  
          Working...