Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • eilosei
    Member
    • Nov 2011
    • 19

    #1

    Help! lost data in fastq file

    I got some Illumina Hiseq result in fastq files from my facility, but the yield is a lot lower than expected.

    For example, the summary file for one sample shows that it contains 225566 +/- 0 clusters (PF), and I expected to get around 225566*32=7 million reads. But the fastq file only includes less than 0.5 million reads. One example read is

    @HWI-1KL117_0134:6:2104:1422:2023#GNCAAT/1
    NTTTTAATGAAAACACGGAAATTAAAAATTCTTGAAGGTGACATCCCTCCA

    Because the sample has index barcode "GCCAAT", is it possible that the facility selected reads with bad barcode "GNCAAT" in stead of "GCCAAT" when demultiplexing? If it is true, is there anyway to rescue my sample?

    Thanks in advance!
  • kopi-o
    Senior Member
    • Feb 2008
    • 319

    #2
    Demultiplexing usually allows for one mismatch and sometimes indels, so it's not surprising that this read would have been considered as matching the barcode. Why don't you go through the whole fastq file and check for the barcodes that appear in the headers with something like

    grep '@' file.fastq | cut -d '#' -f2 | sort | uniq -c

    Maybe your summary was referring to the cluster density for the whole lane, and they had 12 multiplexed samples in it? That would fit approximately with 12*0.5M. 7 million reads for a lane is pretty low, though ...
    Last edited by kopi-o; 11-11-2011, 01:26 PM. Reason: typo

    Comment

    • eilosei
      Member
      • Nov 2011
      • 19

      #3
      Thank you for your quick reply. I tried the command like

      grep '@' 003_s_6_sequence.txt | cut -d '#' -f2 | sort |*uniq -c

      But get the notice like

      -bash: *uniq: command not found

      Beside, the entire fastq file only contains reads from barcode "GNCAAT". As to the summary file, I have three samples in one lane, and each sample has its own summary file after demultiplexing. The PF cluster numbers are similar. So there should be around 10 million PF reads for each, which is still low for HiSeq.

      Comment

      • kopi-o
        Senior Member
        • Feb 2008
        • 319

        #4
        I'm sorry, there was a typo in my reply. The star '*' is not supposed to be there; the command is called uniq. I've removed it.

        Anyway, there is no need for you to run the command if you already know that the entire fastq file contains the same barcode. Then it would appear that the facility has failed to extract the exact-match barcode, or that the second cycle in the index read step went so seriously awry that no base calls could be made.

        Comment

        • kopi-o
          Senior Member
          • Feb 2008
          • 319

          #5
          Also, just a crazy suggestion - why not just ask the facility? :-)

          Comment

          • eilosei
            Member
            • Nov 2011
            • 19

            #6
            Now the command works, and all my three samples from one lane have the same problem. The barcode of each read all carries a mismatch "N" at the second character, e.g. CNATGT, ANAGTG, GNCAAT.

            I will ask the facility to reprocess the demultiplexing step. Hope it's just a computer problem and I can get reads with perfect match barcodes.

            Thanks!

            Comment

            • eilosei
              Member
              • Nov 2011
              • 19

              #7
              Because the facility believed I gave them bad samples, although they said no problem basing on the bioanalyzer result!

              Originally posted by kopi-o View Post
              Also, just a crazy suggestion - why not just ask the facility? :-)

              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
              23 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...