Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • JPC
    Senior Member
    • May 2008
    • 116

    #1

    MiSeq Nextera XT expected output?

    Hello all, how many raw reads am I likely to get from a single MiSeq run with a Nextera XT sample? .....am I being too cynical by assuming that as this is a protocol designed for set-up speed it won't get up to the 30-34M PF reads that I would expect for a normal Paired End run?

    JPC
  • RCJK
    Senior Member
    • May 2009
    • 156

    #2
    I think it is possible to obtain that amount of reads. Maybe slightly less, but not way off, since it's a bit more difficult to get optimised loading due to a wide range of fragment sizes.

    Comment

    • koadman
      Member
      • May 2010
      • 65

      #3
      Hi JPC, in our experience when using the protocol's suggested dilution into hybridization buffer at the last step, the number of reads varies widely by sample type. I'm not sure whether this is due to input material quantitation differences or something else. The protocol suggests the dilution can be changed and presumably this will affect read count. Our group plans to try it this week.

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        PS: Info below is not specific for Nextera runs but a general observation with MiSeq runs.

        MiSeq runs are affected (in terms of yield and sequence quality) to a greater extent if your samples have reduced nucleotide diversity (e.g. 16S). There are other threads (e.g. http://seqanswers.com/forums/showthr...t=20455&page=3) that have information about this known observation specially for long read lengths (2 x 250 bp).

        If you are sequencing normal genomic DNA then you can reasonably expect to recover standard number of reads. If your samples have reduced nucleotide diversity then the number of reads passing filter can potentially experience a significant drop.
        Last edited by GenoMax; 10-17-2012, 04:07 AM. Reason: added clarification

        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
        22 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-28-2026, 09:51 AM
        0 responses
        14 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 11:13 AM
        0 responses
        67 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        47 views
        0 reactions
        Last Post SEQadmin2  
        Working...