Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • NeleZ
    Junior Member
    • Dec 2013
    • 7

    #1

    Narrow vs broad size selection

    Hello,

    I have a question regarding the purpose of the size selection.
    Apart from the more obvious reason to exclude adapter/primer dimers, the mapping of paired-end data requires a defined insert size.

    Now my question:
    Is it preferable to select the fragment-size as narrow as possible (which could make the mapping of paired-end data more accurate, but might lead to the loss of some information!?)
    OR
    would you select a rather broader range (which might allow the identification of more splice-sites, see also https://www.landesbioscience.com/jou...ache=967631737).

    Maybe the mapping works just as fine with a broader range as long as you know and can provide the fragment length distribution!?
    To me it always seems like a trade-off between the two but I don't know what's state-of-the art...
    Since we have the Pippin prep in our lab I have the opportunity to select for a size as narrow as +/-8% but I'm not sure this is desirable...

    Thanks for your help in advance!

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, 10-22-2026, 11:13 AM
0 responses
62 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
44 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
78 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
76 views
0 reactions
Last Post SEQadmin2  
Working...