Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • drea11
    Junior Member
    • Aug 2014
    • 9

    #1

    WGS batch effects

    Hi All,

    I'm relatively new to whole genome sequencing, and have a background in 16S based typing of bacteria using NGS. I am collecting data on a set of closely related organism, using illumina, identifying SNPs, and clustering them into a phylogenetic tree based on the differences between strains. I am wondering whether I need to worry about a 'batch effect' in these samples (either the extraction batch, or sequencing run or library prep or other). If so, it's not really feasible for us to sequence each sample multiple times, what might be the best way to go about first of all, identifying that batch effects may be present, and second, accounting for these in the analysis?

    Thanks!
  • lorendarith

    #2
    Hi, I would generally say that WGS is insensitive to these issues.

    I'm also doing metagenomics and 16S, so I can see where you're coming from... However, you should not see any differences if you resequence a library on the same machine or prepare another one from the same DNA pool, or extract DNA from the same or an identical sample. Eventual differences could come from source DNA degradation over time, changing the polymerases in the PCR (for GC-low and -high regions), sequencing chemistry upgrade and so on... which seems kinda obvious, no? As long as you keep all steps the same, there should not be any differences. Some days the sequencer can have a bad day so you might just get less and cappier data. If something is really wrong with your adapter ligation and subsequent PCR enrichment you can end up with more primer dimers and chimeric sequences, but the biologically relevant and correct sequences should perform equally well as before.

    What you can see is an adapter effect, depending on what kits you use and how experienced you are with plates. Especially if you are using custom designed adapters, there might be some combinations which are less balanced than others, so you'll just end up with a more obvious difference in the number of reads for each particular adapter sequence.

    Just, my experience til now.

    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, 10-22-2026, 11:13 AM
    0 responses
    27 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    20 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
    43 views
    0 reactions
    Last Post SEQadmin2  
    Working...