Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • taylor_wilcox
    Junior Member
    • Oct 2016
    • 3

    #1

    Short mixed amplicon libraries

    I'm interesting in sequencing libraries composed of multiplexed PCR products with amplicon lengths running from 50 - 150 bp. A colleague expressed concern about sequencing bias for shorter amplicons on the Illumina platforms (likely will want to use MiSeq).

    Does anyone have experience sequencing libraries of short, mixed-length amplicons/insert sizes? If so, can you comment on the level of sequencing bias? If sequencing bias was a problem, do have a good working solution (e.g., pooling amplicons of different lengths at different relative molarity)?
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    What kind of sequencing bias are you referring to? If you are going to be mixing products of different length then even the low nucleotide diversity (which may be an issue with amplicon sequencing) would not be a problem.

    Comment

    • taylor_wilcox
      Junior Member
      • Oct 2016
      • 3

      #3
      Sorry I didn't make that clear. I mean a bias towards smaller amplicons (~50 bp) relative to larger amplicons (~ 150 bp). For example, would I expect a large drop in coverage for the 150 bp amplicons relative to the 50 bp amplicons when pooled equimolarly on the same lane?

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        It is true that shorter inserts tend to cluster more efficiently on the flowcell than longer ones. You could use less amounts of shorter ones and try to bias a uniform representation.

        Someone with more practical bench experience may have more specific tips for you now we know what you are working with.

        Comment

        • thermophile
          Senior Member
          • Apr 2015
          • 243

          #5
          length bias still exists on illumina flowcells but it's not anywhere close to as strong as it was with 454. You may need to tweak your load ratios a small amount but not much. 5-10% as a complete guess
          Microbial ecologist, running a sequencing core. I have lots of strong opinions on how to survey communities, pretty sure some are even correct.

          Comment

          • fanli
            Senior Member
            • Jul 2014
            • 197

            #6
            I'm curious about this too - we've held back from running different amplicons together precisely because it'd be a complete shot in the dark as to how much to tweak loading concentrations.

            Here is some data from one of our V1V2 runs (as these will have some naturally occurring length variation). No clear relationship between amplicon size and number of reads output. Note that amplicon size refers to the average size of the largest peak and all libraries were pooled equimolar for sequencing. These are from the Tapestation, fwiw.
            Attached Files

            Comment

            • thermophile
              Senior Member
              • Apr 2015
              • 243

              #7
              My primary type is 16s v4 (~300bp). I've mixed up to 30% of a run with ITS2 (~250-400bp) or custom ~150bp amplicons with no issues and no noticeable decrease in reads for the longer amplicons on the run but I'm looking for a minimum per sample rather than average
              Microbial ecologist, running a sequencing core. I have lots of strong opinions on how to survey communities, pretty sure some are even correct.

              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, 10-15-2026, 10:52 AM
              0 responses
              14 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-14-2026, 05:39 AM
              0 responses
              21 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-13-2026, 09:56 AM
              0 responses
              19 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-09-2026, 11:14 AM
              0 responses
              27 views
              0 reactions
              Last Post SEQadmin2  
              Working...