Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • running findMotifsGenome.pl error

    Hello,

    I am running findMotifGenome.pl in homer package.

    Any help is appreciated!

    With Best!

    Yue Li


    administrator@ACB-Ubuntu:~/homer/bin$ perl findMotifsGenome.pl fox2ClipSeq.hg18.bed hg38 peakAnalysis -size 200 -len 8

    Position file = fox2ClipSeq.hg18.bed
    Genome = hg38
    Output Directory = peakAnalysis
    Fragment size set to 200
    Motif length set at 8,
    Found mset for "human", will check against vertebrates motifs
    sh: 1: bed2pos.pl: not found
    sh: 1: checkPeakFile.pl: not found
    sh: 1: cleanUpPeakFile.pl: not found
    ls: cannot access /home/administrator/homer/.//data/genomes/hg38//preparsed//hg38.*.cgbins: No such file or directory
    Could not find background files for 200 bp fragments
    Below are the sizes that are already available prepared.
    HOMER will now create background files for 200 bp fragments
    To CANCEL and rerun with a differet "-size <#>", hit <CTRL+C> now!
    5
    4
    3
    2
    1
    Preparsing genome for 200 bp fragments...(will probably take 1-5 min)
    sh: 1: preparseGenome.pl: not found
    wc: /home/administrator/homer/.//data/genomes/hg38//preparsed//hg38.200.gcbins: No such file or directory
    Use of uninitialized value $lineCount in numeric lt (<) at findMotifsGenome.pl line 648.
    !!!! Might have something wrong with preparsed files
    !!!! Rerun and add "-preparse" to the command line to force recreation of the files
    sh: 1: resizePosFile.pl: not found
    sh: 1: homerTools: not found
    sh: 1: cleanUpSequences.pl: not found
    sh: 1: removePoorSeq.pl: not found

    Not removing redundant sequences

    sh: 1: homerTools: not found
    sh: 1: freq2group.pl: not found

    Total sequences set to 50000

    Choosing background that matches in CpG/GC content...
    wc: /home/administrator/homer/.//data/genomes/hg38//preparsed//hg38.200.gcbins: No such file or directory
    cat: /home/administrator/homer/.//data/genomes/hg38//preparsed//hg38.200.gcbins: No such file or directory
    sh: 1: makeBinaryFile.pl: not found
    sh: 1: randRemoveBackground.pl: not found
    sh: 1: assignGeneWeights.pl: not found
    Assembling sequence file...
    sh: 1: filterListBy.pl: not found
    Normalizing lower order oligos using homer2
    sh: 1: homer2: not found
    Finished preparing sequence/group files

    ----------------------------------------------------------
    Known motif enrichment
    sh: 1: findKnownMotifs.pl: not found
    ----------------------------------------------------------
    De novo motif finding (HOMER)
    sh: 1: homer2: not found
    cat: peakAnalysis/homerMotifs.motifs*: No such file or directory
    sh: 1: compareMotifs.pl: not found
    Job finished - if results look good, please send beer to ..

    Cleaning up tmp files...

  • #2
    every time open the terminal

    nano ~/.bash_profile

    PATH=$PATH:/home/administrator/homer/bin

    ctrlX

    Y

    enter

    source ~/.bash_profile
    Last edited by yueli; 04-02-2019, 06:42 AM.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin




      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
      04-22-2024, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    59 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    57 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    53 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    56 views
    0 likes
    Last Post seqadmin  
    Working...
    X