Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Normalization of samples before pooling

    Hello everyone!

    Can you kindly tell me what is the best way to normalize the samples before pooling? The application I will be working on is screening different diseased genes for mutations.

    Thanks
    Last edited by discoveradnan; 12-03-2015, 08:31 PM. Reason: typo

  • #2
    I would follow the protocol pertaining to the kit you are using. FOr NextSeq 500 we do Qubit on the libraries and it works beautifully.

    William

    Comment


    • #3
      I usually work with qubit quantifications after the PCR cleanup. Because we normalize based on Molarity, the Qubit conc is converted through this page: http://molbiol.edu.ru/eng/scripts/01_07.html.
      Normaly, the conversion factor is 1.5 but that differs on the average insertion length.

      Then, you must dilute your products to 4, 2 nM to pool them. I do not recomend you to dilute less than 2 nM, and preferably repeat the library prep (or concentrate) before you consider the sample to be pooled.
      Last edited by Ancestro; 03-31-2016, 07:49 AM. Reason: autocorrect fail.

      Comment


      • #4
        Lately we have been pooling without first normalizing the individual libraries. Equimolar amounts of each library are achieved by adjusting the volume added to the pool and then the whole pool is diluted down to ~10nM (or lower for low concentration libraries). The pool is then qPCR'd prior to loading. Using this method we seem to get better balance in our pools, but I'll admit I don't have hard data to back this up.

        Comment


        • #5
          If the concentrations do not vary wildly, I do not see any purpose in normalizing before pooling. We don't do it.

          Comment


          • #6
            We use tap station/bioanalyzer to get mean size of library, use Qubit to get conc. of library, then convert it to molar conc. for pooling.

            Comment


            • #7
              I quantify each library with Qubit, in triplicates and take average. Then calculate how much you need for a 70 ng pool (for example). Change the pool concentration if needed to adjust final volume of pool to 15 or more. Then we do Qubit on the pool and dilute 1:2 and do Qubit again. Dilute only those which are >20 on Qubit. Use the 1:2 pool for qPCR. I think qPCR on the pool works better than doing qPCR on each library.

              Comment

              Latest Articles

              Collapse

              • seqadmin
                Recent Developments in Metagenomics
                by seqadmin





                Metagenomics has improved the way researchers study microorganisms across diverse environments. Historically, studying microorganisms relied on culturing them in the lab, a method that limits the investigation of many species since most are unculturable1. Metagenomics overcomes these issues by allowing the study of microorganisms regardless of their ability to be cultured or the environments they inhabit. Over time, the field has evolved, especially with the advent...
                09-23-2024, 06:35 AM
              • seqadmin
                Understanding Genetic Influence on Infectious Disease
                by seqadmin




                During the COVID-19 pandemic, scientists observed that while some individuals experienced severe illness when infected with SARS-CoV-2, others were barely affected. These disparities left researchers and clinicians wondering what causes the wide variations in response to viral infections and what role genetics plays.

                Jean-Laurent Casanova, M.D., Ph.D., Professor at Rockefeller University, is a leading expert in this crossover between genetics and infectious...
                09-09-2024, 10:59 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by seqadmin, 10-02-2024, 04:51 AM
              0 responses
              11 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 10-01-2024, 07:10 AM
              0 responses
              19 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 09-30-2024, 08:33 AM
              0 responses
              23 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 09-26-2024, 12:57 PM
              0 responses
              17 views
              0 likes
              Last Post seqadmin  
              Working...
              X