Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • efoss
    Member
    • Jul 2011
    • 98

    generating iit file for GSNAP

    gsnap can use information about known splice sites if you give it a .iit file with this format:


    >NM_004448.ERBB2.exon1 17:35110090..35110091 donor 6678
    >NM_004448.ERBB2.exon2 17:35116768..35116769 acceptor 6678
    >NM_004448.ERBB2.exon2 17:35116920..35116921 donor 1179
    >NM_004448.ERBB2.exon3 17:35118099..35118100 acceptor 1179
    >NM_004449.ERG.exon1 21:38955452..38955451 donor 783
    >NM_004449.ERG.exon2 21:38878740..38878739 acceptor 783
    >NM_004449.ERG.exon2 21:38878638..38878637 donor 360
    >NM_004449.ERG.exon3 21:38869542..38869541 acceptor 360

    The number at the end is the length of the intron and it is optional. In this example (which comes from the gmap/gsnap README file), each donor is getting spliced to the following acceptor. But I wonder if this is a requirement. If you have one exon that can get spliced to three different acceptors, does that mean that you have to list that exon three times, once followed by acceptor 1, another followed by acceptor two and the third followed by acceptor 3? Or can I just list all the donor sites and all the acceptor sites without regard to how they are matched up?

    Thank you.

    Eric
  • Richard Finney
    Senior Member
    • Feb 2009
    • 701

    #2
    It would be nice to have a PSL to IIT program (that answered your questions by providing pristine output). Anybody know where one is?

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
      by SEQadmin2



      Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
      ...
      07-09-2026, 11:10 AM
    • SEQadmin2
      Cancer Drug Resistance: The Lingering Barrier to Rising Survival
      by SEQadmin2



      Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

      There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
      07-08-2026, 05:17 AM
    • GATTACAT
      Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
      by GATTACAT
      Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
      07-01-2026, 11:43 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 07-13-2026, 10:26 AM
    0 responses
    27 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-09-2026, 10:04 AM
    0 responses
    37 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-08-2026, 10:08 AM
    0 responses
    24 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-07-2026, 11:05 AM
    0 responses
    34 views
    0 reactions
    Last Post SEQadmin2  
    Working...