Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • panther
    Junior Member
    • Mar 2019
    • 1

    #1

    basic Q about paired end reads from HiSeq

    Hi, I'm new to genomic data and I'm just learning the basics of Illumina HiSeq and the resulting data. There's one thing I'm confused about.

    With paired end reads that don't overlap, do we know the exact insert length without mapping to a reference? Or is it just an estimate based on the distribution of fragment lengths we expect from our library prep protocol?

    I've seen all these posts and videos talking about the insert size of paired end reads, but I couldn't figure out if there's a step in the sequencing that also keeps track of the overall fragment length, which would allow us to know the insert size by subtracting off the length of the two reads (and adapters).

    Thanks!
  • luc
    Senior Member
    • Dec 2010
    • 469

    #2
    With paired end reads that don't overlap, do we know the exact insert length without mapping to a reference? Or is it just an estimate based on the distribution of fragment lengths we expect from our library prep protocol?
    No and then yes.
    Also note that shorter library molecules tend to cluster better than longer molecules.

    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...