Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • hewenjuan
    Junior Member
    • Sep 2017
    • 7

    Library construction primers containing unique molecular barcode

    Hi all,

    We are interested in developing our own library construction method for single cell genomics. We want to incorporate unique molecular barcode in the adapters. Does anyone know where to get primers/oligos containing unique molecular barcode synthesized, or do we have to do it by ourselves?

    If we have to do it by ourselves, does anyone know a good protocol? It looks very complicated.

    Thank you very much in advance!!
  • luc
    Senior Member
    • Dec 2010
    • 469

    #2
    You could incorporate a stretch of "N"s - lets say eighth of them as UMI. This would be by far the cheapest option.

    Comment

    • hewenjuan
      Junior Member
      • Sep 2017
      • 7

      #3
      Thanks, Luc.
      You mean when I order oligo, I can just put "N"s there. The synthesized oligo will then contain random barcodes? Will each individual one be unique? As when we analyze data, the same barcode would indicate the same original template.
      Thank you!!

      Comment

      • luc
        Senior Member
        • Dec 2010
        • 469

        #4
        Yes. That is, what I meant. 10X Genomics uses a 10 nt long UMI for their single-cell kit.
        Last edited by luc; 09-30-2017, 04:31 PM.

        Comment

        • hewenjuan
          Junior Member
          • Sep 2017
          • 7

          #5
          Thanks, Luc.
          I contacted IDT regarding synthesis of these primers containing UMI. They told me that " in 1.0 nmole of oligo with an 8 nt UMI, there would be approximately 6.02*10^14 total molecules but only approximately 65,000 unique sequences". If these UMI are not truly unique, then how can we make sure we are not tagging two different original template molecules with the same UMI?

          Comment

          • cmbetts
            Senior Member
            • Jun 2012
            • 120

            #6
            Each gene is considered separately in regards to the UMIs and the UMIs will be incorporated in a Poisson distribution (a la digital PCR). In the context of single cells, there's never going to be enough copies of a given transcript to saturate the UMI sequences. Will the efficiency of these protocols and copies per cell, it's even unlikely you'll even get duplicated UMI for a single transcript and considering each one uniquely is good enough unless you actually have enough UMIs seen to approach where Poisson gets away from linear. The trickiest problem is accounting for sequencing errors inflating your counts as you sequence deeply, but there are a few software packages that help with that.

            Comment

            • hewenjuan
              Junior Member
              • Sep 2017
              • 7

              #7
              Thanks, cmbetts!

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                by SEQadmin2


                I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.


                Here are nine questions we think about, in roughly the order they matter, before...
                06-18-2026, 07:11 AM
              • SEQadmin2
                From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
                by SEQadmin2


                Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


                The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
                ...
                06-02-2026, 10:05 AM
              • SEQadmin2
                Single-Cell Sequencing at an Inflection Point: Early Impacts of New Platforms and Emerging Trends
                by SEQadmin2


                With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.


                Introduction

                Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...
                05-22-2026, 06:42 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 06-17-2026, 06:09 AM
              0 responses
              21 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 06-09-2026, 11:58 AM
              0 responses
              40 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 06-05-2026, 10:09 AM
              0 responses
              46 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 06-04-2026, 08:59 AM
              0 responses
              49 views
              0 reactions
              Last Post SEQadmin2  
              Working...