Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • aaron.odell
    Junior Member
    • Nov 2013
    • 4

    #1

    GSNAP error

    I am trying to run gsnap on RNA seq data and I receive the following error
    "Unexpected error. Using IIT_read code on a version 1 IIT"

    Here is the command I ran

    gsnap -t 16 -N 0 -m .06 -A sam --quality-protocol=illumina -s refGene.gtf -D GSNAP -d hg19 myFastq > output.sam

    Does anyone know how to correct this error
    I built the genome using gmap_build and did not receive any errors. However, I am unsure that the fasta file I used was in the correct format. Any help would be appreciated

    -Aaron
  • wendy_cityu
    Junior Member
    • Jul 2013
    • 2

    #2
    Have you figured out the reason? I am now facing with the same error.

    Comment

    • aaron.odell
      Junior Member
      • Nov 2013
      • 4

      #3
      My error was because the "-s" flag takes an IIT file instead of a gtf. If you look in the README file that came with GSNAP there is a whole section that tells you how to convert the gtf to the proper format. There are two built in GSNAP programs that you need to run before you can map to your genome/transcriptome. They are "gtf_splicesites" and "iit_store"
      Hope this helps

      -Aaron

      Comment

      • wendy_cityu
        Junior Member
        • Jul 2013
        • 2

        #4
        Yes, I just solved in that way, too. Thanks for the reply, though.

        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, Yesterday, 10:35 AM
        0 responses
        9 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-03-2026, 10:13 AM
        0 responses
        45 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-31-2026, 02:55 AM
        0 responses
        48 views
        0 reactions
        Last Post SEQadmin2  
        Working...