Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • jmw86069
    Member
    • Jun 2009
    • 31

    #1

    TargetScan v6.1 genome coordinates

    I'm trying to find or create genome coordinates for TargetScan v6.1, released March 2012. UCSC provides a track from v5.1, but nothing newer. This thread (link UCSC mailing list) suggests it's trickier than one would think. So before embarking on that quest, I wanted to poll this board to see if anyone already has created genome coordinates from TargetScan v6.1?

    Here is my best guess workflow:
    1. Download UTR_Sequences.txt from TargetScan for the given species, grep out only the taxon ID needed (10090 for mouse from the TargetScanMouse data; 9606 for human from the TargetScanHuman data; etc.)
    2. Create gapped-to-ungapped mapping of the UTR_Sequences.txt data (which is in gapped alignment format) so I can convert the reported TargetScan gapped coordinates to un-gapped UTR coordinates.
    3. Strip out the gaps from each sequence to create an un-gapped UTR FASTA file, then BLAT them to the appropriate genome (mm9, hg18/hg19, etc.), in order to convert UTR ungapped coordinates to genome coordinates. This step seems necessary because the TargetScan UTRs were created using some logic, and aren't directly from any available UCSC track (that I can tell anyway.)
    4. Use the Conserved_Family_Info.txt file for the given organism, which provides gapped UTR coordinates for each predicted miRNA site. Convert each coordinate using the logic above.
    5. (gapped UTR coordinate) --> (ungapped UTR coordinate) --> (genome coordinate)


    I don't know how much I lose by using BLAT to re-align UTRs back to the genome. If anyone has a suggested alternative (e.g. MUMmer?), I'd greatly welcome it! I'm really hoping for well-behaved alignments!
  • DrOM
    Junior Member
    • Jul 2012
    • 5

    #2
    Hallo!

    have you advanced with the genomic coordinates for TargetScan6.2? I think you can skip step #2, since the target file also provides the position in the ungapped UTRs of that species. Therefore it should be ok to strip the gaps of the alignment file, get the genomic coordinates for the UTRs and proceed like you outlined above.

    It would be great if you could share your results!!
    Cheers

    Pablo

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      07-31-2026, 11:01 AM
    • SEQadmin2
      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
      by SEQadmin2


      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

      The systematic characterization of the human proteome has
      ...
      07-20-2026, 11:48 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 08-13-2026, 12:22 PM
    0 responses
    22 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-11-2026, 10:35 AM
    0 responses
    18 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-06-2026, 07:41 AM
    0 responses
    33 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    51 views
    0 reactions
    Last Post SEQadmin2  
    Working...