Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • lfaller
    Junior Member
    • Jul 2017
    • 4

    #1

    Advice needed for --use-bases-mask option (bcl2fastq)

    Hi all,

    A colleague in the lab asked me to demultiplex a recent NextSeq run. She loaded it with samples prepared from two libraries. One library had single indices and one had dual indices. She also prepared two sample sheets for me to use.

    I was able to use the sample sheet for the single-index samples successfully but running bcl2fastq again, this time using the sample sheet for the dual-index samples, did not work (all reads ended up in two large "Undetermined" fastq files).

    Someone suggested I use the --use-bases-mask option for bcl2fastq but I am not entirely sure how to set it up.

    The information in the RunInfo.xml file is as follows:

    Code:
    ...
        <Reads>
          <Read Number="1" NumCycles="147" IsIndexedRead="N" />
          <Read Number="2" NumCycles="12" IsIndexedRead="Y" />
          <Read Number="3" NumCycles="12" IsIndexedRead="Y" />
          <Read Number="4" NumCycles="147" IsIndexedRead="N" />
        </Reads>
        <FlowcellLayout LaneCount="4" SurfaceCount="2" SwathCount="3" TileCount="12" SectionPerLane="3" LanePerSection="2">
          <TileSet TileNamingConvention="FiveDigit">
            <Tiles>
              <Tile>1_11101</Tile>
              <Tile>1_21101</Tile>
    ...
    The indices my colleague gave me in the sample sheet are eight bases long so I tried this approach:

    Code:
    --use-bases-mask Y147,I8nnnn,I8nnnn,Y147
    However, as before, all reads ended up in the Undetermined files.

    My questions:

    1) Is using --use-bases-mask the best approach?
    2) I read somewhere on here that the sample sheets can be combined so that bcl2fastq only needs to be run once -- is that a preferable approach?

    By the way, for all of this I am using bcl2fastq v2.17.1.14.

    Thank you in advance, any advice would be appreciated!
  • fanli
    Senior Member
    • Jul 2014
    • 197

    #2
    Originally posted by lfaller View Post
    Code:
    --use-bases-mask Y147,I8nnnn,I8nnnn,Y147
    However, as before, all reads ended up in the Undetermined files.
    Maybe try looking in the index read files and see if the 8-base barcodes are indeed at the beginning of the index reads.
    Code:
    --create-fastq-for-index-reads
    Originally posted by lfaller View Post
    1) Is using --use-bases-mask the best approach?
    Seems appropriate to me.

    Comment

    • kcchan
      Senior Member
      • Jul 2012
      • 186

      #3
      Did you remember to reverse complement the index2s?

      Comment

      • lfaller
        Junior Member
        • Jul 2017
        • 4

        #4
        Thank you for suggestion!

        I went back to the lab tech and asked her to take a critical look at the indices. She regenerated the file using the Illumina Experiment Manager and now it worked. I believe she messed up the file she gave me the first time around...

        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, Today, 11:13 AM
        0 responses
        11 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Today, 10:48 AM
        0 responses
        10 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        32 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        40 views
        0 reactions
        Last Post SEQadmin2  
        Working...