Header Leaderboard Ad

Collapse

Short reads - dodgy consumables?

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Short reads - dodgy consumables?

    After a short spell of good results, again we're getting way short reads on our 454 Titanium WGS runs. Last time this was down to dodgy consumables and Roche put a release out admitting there was a QC problem. Anyone else having problems recently?

  • #2
    Yes, but not very consistent so this could be due to sample problems.

    Comment


    • #3
      Same for us, we've had 5-6 runs of very short reads (250bp average) in the past 3 weeks after 3-4 months of 400+bp (many samples had previously been successfully sequenced so not sample related)

      Comment


      • #4
        Ah.

        Perhaps it would be useful to compare lot numbers on consumables, do you have them to hand?

        Comment


        • #5
          Since we started using Seq kit 93801620 (for which they announced a new formulation of their substrate solution) although correlation is not perfect.

          Comment


          • #6
            The engineer came:

            It seems some of the tubes inside were dirty and wash flow may have been insufficient which means removal of residual dNTP after each cycle would be incomplete and so as the reads progress, there is increasing corruption of the read sequence due to overlapping reads after displacement of the end of the strand 'forwards' by illegitimate insertion of bases that should not be available in the next cycle (if I've understood correctly), a phenomenon called read-forward. Apparently Roche's analysis of the data suggested that this was indeed the problem.

            This suggests to us we need to make sure the tubes are replaced at no more than 12 mo intervals and possibly as little as 6 mo.

            (Edited this post for clarity)
            Last edited by nickloman; 11-17-2010, 06:39 AM.

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Targeted Sequencing: Choosing Between Hybridization Capture and Amplicon Sequencing
              by seqadmin




              Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches...
              03-10-2023, 05:31 AM
            • seqadmin
              Expert Advice on Automating Your Library Preparations
              by seqadmin



              Using automation to prepare sequencing libraries isn’t a new concept, and most researchers are aware that there are numerous benefits to automating this process. However, many labs are still hesitant to switch to automation and often believe that it’s not suitable for their lab. To combat these concerns, we’ll cover some of the key advantages, review the most important considerations, and get real-world advice from automation experts to remove any lingering anxieties....
              02-21-2023, 02:14 PM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 03-17-2023, 12:32 PM
            0 responses
            7 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 03-15-2023, 12:42 PM
            0 responses
            17 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 03-09-2023, 10:17 AM
            0 responses
            66 views
            1 like
            Last Post seqadmin  
            Started by seqadmin, 03-03-2023, 12:03 PM
            0 responses
            64 views
            0 likes
            Last Post seqadmin  
            Working...
            X