Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • cascoamarillo
    Senior Member
    • Oct 2010
    • 164

    #1

    sharing flowcell/lanes

    Hi all,

    One basic question; is it possible to share one flowcell (7 diferent lanes + control) for HiSeq with paired-end library samples (6 lanes) and one sample of small RNA library (1 lane) which doen't require paired-end rxn?

    I guess that maybe the small RNA library needs to be run as a paired-end; could this to be done with the small RNA adapters used in this thread and the HiSeq platform:

    Bridged amplification & clustering followed by sequencing by synthesis. (Genome Analyzer / HiSeq / MiSeq)


    Small RNA oligonucleotide sequences

    RT Primer
    5' CAAGCAGAAGACGGCATACGA

    5' RNA Adapter
    5' GUUCAGAGUUCUACAGUCCGACGAUC

    3' RNA Adapter
    5' P-UCGUAUGCCGUCUUCUGCUUGUidT

    Small RNA PCR Primer 1
    5' CAAGCAGAAGACGGCATACGA

    Small RNA PCR Primer 2
    5' AATGATACGGCGACCACCGACAGGTTCAGAGTTCTACAGTCCGA

    Small RNA Sequencing Primer
    5' CGACAGGTTCAGAGTTCTACAGTCCGACGATC
  • cascoamarillo
    Senior Member
    • Oct 2010
    • 164

    #2
    Ok, this is what I found:

    Apparently, the adapters for original small RNA library are for single read (SR). The new TruSeq adapters are for paired end read (PE). So there is two types of flow cells (I didn't know that; I thought the difference was based on the chemistry) SE and PE; where SR adapter library can form cluster on SR flow cell ONLY, and PE adapter library can form cluster on both SR or PE flow cell.

    But I don't really understand why SR library is not able to be clustered on a PE flow cell, the PE flow cell should have the same imbobilised oligos in the surface, shouldn't it?

    Thanks.

    Comment

    Latest Articles

    Collapse

    • 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
    • SEQadmin2
      New Genomics Technologies Take Aim at Long-Standing Limits
      by SEQadmin2


      Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

      We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
      ...
      09-28-2026, 10:25 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Yesterday, 11:13 AM
    0 responses
    19 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, Yesterday, 10:48 AM
    0 responses
    18 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-15-2026, 10:52 AM
    0 responses
    36 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-14-2026, 05:39 AM
    0 responses
    42 views
    0 reactions
    Last Post SEQadmin2  
    Working...