Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dgorelik
    Junior Member
    • Aug 2013
    • 4

    #1

    HTSeq-Count settings

    Hey all,

    I was wondering if anyone knew the minimum intersection for a read to be counted in the attached scenario (bottom) in the intersection-nonempty setting, and if there is anyway to change it?



    Thank you so much!
    Attached Files
  • dgorelik
    Junior Member
    • Aug 2013
    • 4

    #2
    Does anybody know?

    Comment

    • crazyhottommy
      Senior Member
      • Apr 2012
      • 187

      #3
      I assume it is 1 bp. I do not know how to change it...

      Comment

      • dgorelik
        Junior Member
        • Aug 2013
        • 4

        #4
        So, that means, for example, if a read begins with A, it will map to any genes that end with A?

        That doesn't seem to be very useful...

        Comment

        • jparsons
          Member
          • Feb 2012
          • 62

          #5
          It's not quite as bad as you make it out to be, dgorelik: If a read maps to position 1000-1100 (with the specific 100mer sequence which that entails), it will add a count for a gene which ends at position 1000.

          HTSeq isn't doing anything with the base content of the read - only the genomic positions to which those reads map.

          Comment

          • dgorelik
            Junior Member
            • Aug 2013
            • 4

            #6
            Okay, I understand. Thanks for clearing that up.

            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
            • 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

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, Today, 10:13 AM
            0 responses
            10 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            23 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            19 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-23-2026, 11:41 AM
            0 responses
            17 views
            0 reactions
            Last Post SEQadmin2  
            Working...