Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • jomare1188
    Junior Member
    • Jul 2017
    • 5

    #1

    NextSeq 550 Fastq header

    Hi, im working with PE Nextseq 550 data

    I know that there are 12 inline barcodes from 5 to 8 bp for my data

    the reads fastq headers shows 57 different dual index sequences (all 8 bp each one) with CGGGGGGG+TGCTTCCA the most prevalent being in the 98% of the total reads

    something like this:
    @NB501358:172:HTJY7BGX2:1:11101:17581:139461:N:0:CGGGGGGG+TGCTTCCA

    does someone know what the 57 sequences means?

    thanks
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Are you sure about inline barcodes?

    The example you posted above is standard Illumina index sequences for a dual indexed run. It is common to see a mishmash of combinatorial index sequences (besides those known to be there) in sequence data. They represent errors among other things. I am not sure why you received 57 combinations (it is as if they gave you the remaining data after they took what they wanted). Was this sample run with others that did not belong to you?

    Comment

    • jomare1188
      Junior Member
      • Jul 2017
      • 5

      #3
      Thanks for your answer!

      Yes i'm sure about the inline barcodes

      Yes this data was provided by a external lab most probably was run with other data

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        If "CGGGGGGG+TGCTTCCA" is 98% of the data then you should remove and ignore the rest. You have no idea what is in there if your sample was part of a larger pool. If you are able to recognize the inline barcodes conclusively then you could go fishing in the remainder of the data.

        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
        • SEQadmin2
          Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
          by SEQadmin2



          Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
          ...
          07-09-2026, 11:10 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 08-03-2026, 10:13 AM
        0 responses
        15 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-31-2026, 02:55 AM
        0 responses
        32 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-24-2026, 12:17 PM
        0 responses
        23 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-23-2026, 11:41 AM
        0 responses
        21 views
        0 reactions
        Last Post SEQadmin2  
        Working...