Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ox_zoo
    Junior Member
    • Nov 2016
    • 5

    #1

    Low QC scores?

    I have just set up my very first sequencing experiment on the Next-Seq 500. It is now 45 cycles into PE sequencing, however it seems that my QC scores are a bit low. I only have a % >= Q30%: 25.2%

    I have around:
    280 million reads in the QC 10 bin.
    25 million in the QC 20 bin
    8 million in the QC 25 bin
    65 million in QC 30 bin
    44 million in QC 35 bin.

    Is this a bad result? Apologies for my stupidness, just was wondering whether data could be salvaged from this?
  • ox_zoo
    Junior Member
    • Nov 2016
    • 5

    #2
    Yes, now it has finished and the QC is only 15.2.

    The machine also has a warning message on two of the lanes:

    camera disabled:failed to detect clusters


    Does this mean that the cameras are not working properly?

    Thanks

    Comment

    • GenoMax
      Senior Member
      • Feb 2008
      • 7142

      #3
      Probably. You should contact Illumina tech support. They can take a look at your sequencer remotely to diagnose the problem.

      If your instrument is not directly accessible over the network then you will need to send them some diagnostic files.

      Comment

      • ox_zoo
        Junior Member
        • Nov 2016
        • 5

        #4
        Thanks for your reply.

        Yes I will do that - unfortunately since its a weekend they cannot reply.

        I was thinking - if clusters are not formed in those two particular areas, would the cameras be disabled? My pooled library concentration was sufficient, so I did not anticipate any problems. Also, if the cluster density is low then I am not sure how QC would be affected..

        Many thanks
        Last edited by ox_zoo; 11-19-2016, 07:39 AM.

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #5
          What was the cluster density for this run?

          If the run was borderline overclustered to begin with, it is possible that sequencer lost the ability to distinguish the clusters over time (they become fatter). There is also the possibility of this being some sort of a hardware issue.

          Comment

          • ox_zoo
            Junior Member
            • Nov 2016
            • 5

            #6
            The cluster density for the four lanes range from 0-250k/mm2.

            The lanes:
            Lane 1: 235 ±41
            Lane 2: 237 ±38
            Lane 3: 212 ±56
            Lane 4: 230 ±35

            I hope this helps.

            Comment

            • GenoMax
              Senior Member
              • Feb 2008
              • 7142

              #7
              This run is borderline overclustered (as I recollect for NextSeq optimal cluster density is 170-220 K cluster/mm^2).

              Since there is nothing to lose at this time contact tech support and see what they say. You may have to eat the cost on this one and re-run.

              Comment

              • bini
                Junior Member
                • Jul 2018
                • 2

                #8
                Hi, How was this error fixed?

                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
                21 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-31-2026, 02:55 AM
                0 responses
                35 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-24-2026, 12:17 PM
                0 responses
                25 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...