Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • epistatic
    Senior Member
    • Mar 2009
    • 129

    #1

    TruSeq methylated adapters?

    Sorry for post, solved with quick phone call to Illumina.

    For anyone else interested, the TruSeq adapters that come in the kits are methylated, so they can be used for bisulfite conversion prior to the PCR step. This is great because we can now take advantage of the multiplexing.
    Last edited by epistatic; 05-20-2011, 08:21 AM.
  • lterhune
    Member
    • Sep 2011
    • 19

    #2
    Hi there, have you tried the bisulfite conversion after TruSeq and been successful? Because we just tried after our first TruSeq library-- which looked great on a gel-- and got nothing after conversion! We had been using the same Zymo kit for months with a homemade Illumina pair-end library protocol without problems. We called Illumina like you did and expected it to work. If it worked for you maybe it was a problem with our kit or library.

    Comment

    • atgc1
      Junior Member
      • Mar 2013
      • 1

      #3
      The Truseq LT kit adapters are methylated but the HT kit adapters are NOT methylated

      Comment

      • SeqR&D
        Member
        • Sep 2010
        • 26

        #4
        I have perfomed BSC on TruSeq libraries several times and have had no problems other than losses/degradation. I recently tested BSC kits (Promega methyledge, Qiagen Epitect fast, and both the Zymo Gold/lightning kits (still waiting for my Epigentek kit)) on both a ~1kb fragment and gDNA. Overall the Promega kit had the least fragmentation and was similar in yield to the Zymo kits (the lightning kit was better than the gold kit for fragmentation). Qiagen had the worst recovery at about 60% (others were around 80%), but I did not use the carrier RNA supplied with the kit as i was converting 500ng (it was also the most time consuming purification).

        Since I can't figure out how to post an image here...if you care to see my results, just give me your email address and I'll send it to you. I don't work for any of these companies.

        Comment

        • Lovro
          Member
          • Mar 2015
          • 19

          #5
          Hi.

          I would like to bisulfite sequence (Illumina platform) selected loci on human genome.
          I have ordered custom hybridization probes from IDT in order to enrich the human DNA. I was under impression that I also need methylated adapters/indexes in order to be able to bisulfite treat the multiplexed libraries.
          Are you saying there is no need for the latter ?
          Idealy i would like to multiplex 96 probands, however 48 would be acceptable.

          Besides IDT which offers custom oligos, I have also found stock methylated adapters here:


          Does anyone know of another company supplying methylated Illumina adapters/indexes?
          Are they needed at all?

          TNX for help!

          Comment

          • SeqR&D
            Member
            • Sep 2010
            • 26

            #6
            Hi

            Yes, you definitely need methylated adapters...Assuming you are BSC the libraries before adding the adapters, which is likely no.

            What is your custom hybridization probe plexity? How many probes? Unless you have some amazing process, anything below 20k probes will likely not yield much product after enrichment and BSC...you'll sequence more duplicates than not. Maybe you have a pooling plan to increase the amount of DNA going into BSC?

            Hasn't anyone made this assay kit yet?

            I don't know anywhere else to get specific methylated adapters.

            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, 08-13-2026, 12:22 PM
            0 responses
            31 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-11-2026, 10:35 AM
            0 responses
            24 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-06-2026, 07:41 AM
            0 responses
            38 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            51 views
            0 reactions
            Last Post SEQadmin2  
            Working...