Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • syintel87
    Member
    • Dec 2012
    • 81

    #1

    HTSeq: union or intersection-empty or intersection-strict

    While running HTSeq, which option is recommended to use among -m union, -m intersection-empty, and -m intersection-strict?

    The below is one of the results I've got. Would you please give me a tip about with which data I will have to analyze in the next step? I am thinking of adopting DESeq or EdgeR.

    CASE1: -m union
    no_feature 4152
    ambiguous 391
    too_low_aQual 0
    not_aligned 0
    alignment_not_unique 4110

    CASE2: -m intersectioin-nonempty
    no_feature 4223
    ambiguous 249
    too_low_aQual 0
    not_aligned 0
    alignment_not_unique 4110

    CASE3: -m intersection-strict
    no_feature 7797
    ambiguous 221
    too_low_aQual 0
    not_aligned 0
    alignment_not_unique 4110
  • Simon Anders
    Senior Member
    • Feb 2010
    • 995

    #2
    I haven't used anything else than "union" since long, and, admittedly, I would find it hard to now come up with good examples where the intersection modes would be preferable in practice. (When I wrote htseq-count two years ago, that was not so clear yet, of course.)

    Comment

    • syintel87
      Member
      • Dec 2012
      • 81

      #3
      Originally posted by Simon Anders View Post
      I haven't used anything else than "union" since long, and, admittedly, I would find it hard to now come up with good examples where the intersection modes would be preferable in practice. (When I wrote htseq-count two years ago, that was not so clear yet, of course.)
      Thank you!

      I have one more question.
      An option "-s no" seems more conservative, since this means the strandedness is not certain. (Is this right?)

      Then, when the truth is "-s no", what if is "-s yes" chosen in running htseq-count?
      Also, when the truth is "-s yes", what if is "-s no" chosen in running htseq-count?
      What are expected results? How much would the result be biased?


      Thank you in advance!

      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, Today, 10:35 AM
      0 responses
      4 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-06-2026, 07:41 AM
      0 responses
      23 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      41 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-31-2026, 02:55 AM
      0 responses
      47 views
      0 reactions
      Last Post SEQadmin2  
      Working...