Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • flyingoyster
    Member
    • Aug 2011
    • 10

    #1

    "not_aligment" from the output of HTseq-count

    What's the meaning of "not_alignment" from the output of HTseq-count? The manual says it is the "reads in the Sam/Bam file without alignment". Does this mean the reads that are not mapped to the reference? or anything else? Thanks!
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    Yeah, these are just reads that didn't align. Whether the count for this is 0 or not will depend on the aligner that you're using (some don't put unaligned reads in the output SAM/BAM file, others do).

    Comment

    • flyingoyster
      Member
      • Aug 2011
      • 10

      #3
      Assuming that the file I used for input of HTseq-count includes the unaligned reads in the output BAM file, But the number of "no_alignment" reads doesn't match the number of reads not mapped to the reference. Any idea about this? Thanks!

      Comment

      • Simon Anders
        Senior Member
        • Feb 2010
        • 995

        #4
        it should match. Maybe it's paired-end? (htseq-count counts read pairs, not reads)

        Comment

        • dpryan
          Devon Ryan
          • Jul 2011
          • 3478

          #5
          @flyingoyster: Try using the -o option to see what's going on in your case.

          Comment

          • flyingoyster
            Member
            • Aug 2011
            • 10

            #6
            @Simon Anders, Yes, My data is paired-end. If HTseq-count counts read pairs, not reads, that makes sense. Thanks a lot!
            @dpryan, I used Galaxy server, so not be able to choose options.

            If I want to calculate the number of reads within genes, is it right to substract the number of no_feature reads from the total number of mapped reads? Thanks!

            Comment

            Latest Articles

            Collapse

            • SEQadmin2
              16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
              by SEQadmin2




              NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
              Today, 06:46 AM
            • SEQadmin2
              Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
              by SEQadmin2



              Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

              Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
              ...
              10-14-2026, 09:55 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 10-28-2026, 09:57 AM
            0 responses
            24 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-28-2026, 09:51 AM
            0 responses
            15 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-22-2026, 11:13 AM
            0 responses
            68 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-22-2026, 10:48 AM
            0 responses
            48 views
            0 reactions
            Last Post SEQadmin2  
            Working...