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
                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
              18 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 04-10-2024, 10:19 PM
              0 responses
              22 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 04-10-2024, 09:21 AM
              0 responses
              16 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 04-04-2024, 09:00 AM
              0 responses
              47 views
              0 likes
              Last Post seqadmin  
              Working...
              X