Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • rgejman
    Junior Member
    • Nov 2010
    • 4

    TruSeq v3 Cluster Kits with TruSeq SBS kits?

    Hi all,

    Has anyone experimented with using TruSeq SBS kits (i.e. not v3 SBS kits) to sequence TruSeq v3 Cluster Kits and flow cells?. I have heard through the grapevine that it can be done and I was hoping that this might resolve a cluster kit / SBS kit mismatch problem.

    Thanks!
  • GW_OK
    Senior Member
    • Sep 2009
    • 411

    #2
    Didja try calling Illumina tech support?

    Comment

    • bkingham
      Member
      • May 2008
      • 11

      #3
      I haven't done it... but did ask the question. It can be done with no problem.
      The v3 cluster kit advancement is more reads (bigger flow cell/more clustering real estate), and improved GC resolution (chemistry changes). The v3 sequencing kit advancement is simply better stability, you can load 209 cycles of ICR, rather than split for a 2x101. TruSeq v1 seq kits can be used with v3 cluster kits with no reduction in q scores (presumably), you just have to split ICR for a 2x101

      Comment

      • pmiguel
        Senior Member
        • Aug 2008
        • 2328

        #4
        Are there not issues with switching from v1 -> v3 requiring an initial "double priming" of fluids lines that blows an extra 4 cycles worth of reagents? I guess if you have not run v3 chemistry yet it doesn't matter. But if you were thinking about switching back and forth then this could be an issue.

        --
        Phillip

        Comment

        • rgejman
          Junior Member
          • Nov 2010
          • 4

          #5
          Does this "double priming" have to happen once or every time you load a v1 vs. v3 flow cell? I actually buy 200 cycle kit (actually 202 cycle kits) and aliquot them into 4x 50 cycle kits (for which I can actually run 51 cycles—works like a charm). If double priming happens every time I switch then this will not be feasible...

          Comment

          • pmiguel
            Senior Member
            • Aug 2008
            • 2328

            #6
            It is the SBS kit, not the flowcell that is the issue.

            From what we have been told, a double prime needs to be done every time one uses v3 chemistry in an instrument that used v1 chemistry for its previous run.

            The 200 cycle kits are supposed to be sufficient for a 4 (single prime)+ 101+ 7 +101 -- so roughly 213 cycles worth. A 50 cycle kit would (by the same logic) be 4 + 50 +7 = 61 cycles worth.

            --
            Phillip

            Comment

            Latest Articles

            Collapse

            • 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
            • SEQadmin2
              Cancer Drug Resistance: The Lingering Barrier to Rising Survival
              by SEQadmin2



              Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

              There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
              07-08-2026, 05:17 AM
            • GATTACAT
              Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
              by GATTACAT
              Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
              07-01-2026, 11:43 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 07-13-2026, 10:26 AM
            0 responses
            28 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-09-2026, 10:04 AM
            0 responses
            37 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-08-2026, 10:08 AM
            0 responses
            25 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-07-2026, 11:05 AM
            0 responses
            35 views
            0 reactions
            Last Post SEQadmin2  
            Working...