Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • gmap_build error

    Hey guys,

    I am trying to build a custom reference (mm9+ERCC spike-in) to reproduce some single cell RNA-seq results. I appended the mm9 genome (as a fasta file) with the ERCC sequences (also as fasta) and run the following command:

    Code:
    gmap_build -d mm9_ERCC92 mm9_ERCC92.fa -k 15 -D ~/stefan/scLVM/
    All goes well until:

    Building suffix array
    SACA_K called with n = 2725848238, K = 5, level 0
    /usr/local/bin/gmapindex -d mm9_ERCC92 -F /stefan//scLVM//mm9_ERCC92 -D /stefan/scLVM//mm9_ERCC92 -S failed with return code 9 at /usr/local/bin/gmap_build line 375.

    Any ideas what could be going on here?

  • #2
    Hi Stefan,

    only a shot in the dark: did you check the fasta's window length? Try fastx-toolkit's fasta_formatter:
    Code:
    fasta_formatter -w 60 -i mm9_ERCC92.fa -o mm9_ERCC92_w60.fa
    diff -s mm9_ERCC92.fa mm9_ERCC92_w60.fa
    Cheers,
    Michael

    Comment


    • #3
      Hi Michael,

      I just compared the two files and they are indeed different.

      Comment


      • #4
        Thinking about it twice, the two files can differ and still it will not work (if the window-length is constant but not 60 nts).

        Just check the line length visually with the first ERCC-transcript (should be ERCC-00002):

        Code:
        grep -A1 -B1 ERCC-00002 mm9_ERCC92.fa

        Comment


        • #5
          Okay, the ERCC sequences are shorter than 60 nts. So gmap_build can't handle that? But it should work with the the corrected file mm9_ERCC92_w60.fa?

          Edit: Alright, I get the same error with the formatted file... I really appreciate the help though. Maybe you or someone else has another idea?

          Edit 2: The error seems to be in the suffix array construction. Is it really necessary to build that or does it only slow things down later?
          Last edited by StefanF; 09-07-2015, 12:00 AM. Reason: Update

          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, 05-02-2024, 08:06 AM
          0 responses
          16 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-30-2024, 12:17 PM
          0 responses
          20 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-29-2024, 10:49 AM
          0 responses
          25 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-25-2024, 11:49 AM
          0 responses
          28 views
          0 likes
          Last Post seqadmin  
          Working...
          X