Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • golharam
    Member
    • Dec 2009
    • 55

    #1

    MiSeq FastQ Header for pair-end data

    So the Miseq fastq header for pair-end data has changed. I used to see a /1 or /2 at the end of the read name. Now I get something like this for the first read:

    @HWI:1:X:2:1101:1094:2143 1:N:0: CGGCTATG-ATAGAGGC

    and this for the second read:

    @HWI:1:X:2:1101:1094:2143 4:N:0: CGGCTATG-ATAGAGGC

    I've seen the the number 3 or 4 in the second read but not sure what they mean, and haven't seen an explanation anywhere. Does anyone know what this number signifies?
  • Brian Bushnell
    Super Moderator
    • Jan 2014
    • 2709

    #2
    That's good to know; I had only seen 2 for read 2 - now I need to update my header-detection routines. I imagine it has to do with how the machine counts sequencing phases for dual-index:

    1: Read 1
    2: Barcode 1
    3: Barcode 2
    4: Read 2

    It's not unusual for Illumina to randomly change stuff like that with software updates, which is pretty annoying.

    Comment

    • GenoMax
      Senior Member
      • Feb 2008
      • 7142

      #3
      Can you tell us where the data was analyzed, on instrument/in BaseSpace? Was the analysis done using standard parameters (i.e. no separate fastq files for tag reads).

      Comment

      • kcchan
        Senior Member
        • Jul 2012
        • 186

        #4
        If the headers are starting with @HWI it's almost certainly generated using BCL2FASTQ and not MiSeq Reporter, which uses @M0xxxx.

        Comment

        Latest Articles

        Collapse

        • 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
        • SEQadmin2
          New Genomics Technologies Take Aim at Long-Standing Limits
          by SEQadmin2


          Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

          We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
          ...
          09-28-2026, 10:25 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 10:52 AM
        0 responses
        9 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        19 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-13-2026, 09:56 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-09-2026, 11:14 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Working...