Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • puzzle with gmapper -M mirna (shrimp)

    Hi everyone,
    i am mapping short reads from ion torrent PGM. Reads are QV~20 and 16-155 length.
    In FastQC appears this as the highest represented read:
    TGAGGTAGTAGGTTGTGTGGTT 19528counts

    Runing a quick blast it matches 100% bta-let-7b (bta my sp of interest):
    UserSe 1 ugagguaguagguugugugguu 22
    bta-let-7b 1 ugagguaguagguugugugguu 22

    Of course I can't do this with all my reads, so i mapped them to all ncRNAs and mirna-stem-loops for bos taurus, using shrimp in mirna mode:

    gmapper-ls myfile.fa P1_adapter.fa bta-ncRNAs.fa -M mirna >myfile.out 2>myfile.log

    After counting the repeated elements in the RNAME coulumn of the SAM file, bta-let-7b appears nowhere and neither the corresponding miRNAs for the other highly counted reads.

    I have tried this again using same parameters with only stem loops and then only mature mirna sequences.

    In all trials the resuls were the same.

    Hope you can come up with soemthing, i will keep trying other settings for gmapper and I will let you know how it went.

    Thaks!
    Last edited by Sergio.pv; 11-21-2013, 05:57 AM.

  • #2
    I did the following, as a test:
    first, i use the above metioned sequences (identical as you can see)
    >bta-let-7b MIMAT0004331
    UGAGGUAGUAGGUUGUGUGGUU
    >dummy
    UGAGGUAGUAGGUUGUGUGGUU

    gmapper-ls dummy-seq.fa dummy-let-7b.fa -N 12 -o 10 -h 80% >map.out 2>map.log

    Output:
    HD VN:1.0 SO:unsorted
    @SQ SN:bta-let-7b LN:22
    @PG ID:gmapper VN:2.2.3 CL:gmapper-ls dummy-seq.fa dummy-let-7b.fa -N 12 -o 10 -h 80%
    dummy 0 bta-let-7b 1 250 22M * 0 0 NGAGGNAGNAGGNNGNGNGGNN *

    Which is ok.

    But if I change the dummy sequence (U -> T), into the original output of the sequencer (Us as Ts) i don't get results:
    @HD VN:1.0 SO:unsorted
    @SQ SN:bta-let-7b LN:22
    @PG ID:gmapper VN:2.2.3 CL:gmapper-ls dummy-seq.fa dummy-let-7b.fa -N 12 -o 10 -h 80%

    It seems that the use of Ts is not computed. Is that correct?, is there an option to modifify that?

    Best!

    Comment


    • #3
      Ok, to make it work i converted U into T and it worked.
      if it is any use, with fastx tool kit:

      fasta_nucleotide_changer -v -i bta-stem-loops.mirbase20.fa -o bta-stemloops.fa -d

      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, Today, 08:47 AM
      0 responses
      10 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-11-2024, 12:08 PM
      0 responses
      60 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  
      Working...
      X