Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 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!

  • #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

    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM
    • seqadmin
      Strategies for Sequencing Challenging Samples
      by seqadmin


      Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
      03-22-2024, 06:39 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    30 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    32 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    28 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    53 views
    0 likes
    Last Post seqadmin  
    Working...
    X