Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • sebl
    Member
    • Mar 2014
    • 26

    #1

    Minimum run output and quality

    Hello,

    I hope this is the right place to ask this.

    I was asked to write the terms for a tender for a NGS service provider for our institute.

    We aim to work mainly with whole genome sequencing/re-sequencing of bacteria and viruses.

    The question is how may I specify the minimum parameters of output and quality below which it would be reasonable to require (demand?) that the service provider perform a run again without charge?

    I mean, what is the minimum % of the expected output for any type of run (say, Illumina) below which a run is considered invalid? Same for average quality? Other parameters that should be included (run parameters)?

    Thank you!
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Take a look at http://allseq.com/ and https://genohub.com/ to get an idea of what is out there. The guarantee's are going to vary from provider to provider.

    Yields from typical Illumina runs are published in the specs for each instrument (e.g. http://www.illumina.com/systems/hise...fications.html you can search for other sequencers). You need to keep in mind that these specs are for "normal" (uniform A/C/T/G distribution) samples and while they are achievable with regular samples the quality of the libraries has to be excellent to get this sort of output. You have not said if you will be making the libraries or expect the provider to make them. Quality libraries will generate quality output.

    Ultimately the level of service may depend of the volume of samples you have available. Larger volumes will give your more flexibility. But if the volume is low then don't expect a lot of leeway.

    Comment

    • sebl
      Member
      • Mar 2014
      • 26

      #3
      Hi,

      Thanks for the links. From Genohub:

      Unless otherwise specified in the quote, the provider agrees to deliver pass filter reads that are at least 85%.
      So, if I got it right, let's say we are talking about a Miseq run with V2 chemistry. Illumina specs. are
      >75% bases higher than Q30 at 2x250 bp
      . So the sequencer in Genohub would guarantee for minimum 85% or of the 75% expected output?

      Comment

      • sebl
        Member
        • Mar 2014
        • 26

        #4
        Oh, and I mean that lib prep would be included in the service.

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #5
          Originally posted by sebl View Post
          Hi,

          So, if I got it right, let's say we are talking about a Miseq run with V2 chemistry. Illumina specs. are . So the sequencer in Genohub would guarantee for minimum 85% or of the 75% expected output?
          Yes. Achievable with normal/good libraries (no low nucleotide diversity).

          Be sure to include sample QC in your request since that will likely be an added cost. It may sometimes be worth paying that upfront since you will know which samples are not worth processing for libraries.

          Comment

          • sebl
            Member
            • Mar 2014
            • 26

            #6
            Good point, thanks!

            Comment

            Latest Articles

            Collapse

            • SEQadmin2
              Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
              by SEQadmin2



              CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

              Despite this, “CRISPR helped turn genome editing from a specialized technique into
              ...
              07-31-2026, 11:01 AM
            • SEQadmin2
              Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
              by SEQadmin2


              Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

              The systematic characterization of the human proteome has
              ...
              07-20-2026, 11:48 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 08-06-2026, 07:41 AM
            0 responses
            22 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            33 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            43 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            26 views
            0 reactions
            Last Post SEQadmin2  
            Working...