Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • ATAC-Seq large fragments

    Hi All,
    We've been trying to optimize ATAC-Seq on sorted embryonic cell populations and have run into a possible problem. After library prep we QC with a BioAnalyzer and see a large peak at around 2000bp. This doesn't change with increased amounts of enzyme or increased incubation. Any thoughts?
    Attached Files
    Last edited by cfuttner; 02-25-2015, 07:50 AM.

  • #2
    Originally posted by cfuttner View Post
    Hi All,
    We've been trying to optimize ATAC-Seq on sorted embryonic cell populations and have run into a possible problem. After library prep we QC with a BioAnalyzer and see a large peak at around 2000bp. This doesn't change with increased amounts of enzyme or increased incubation. Any thoughts?
    I have been using ES cells and for a while I was getting profiles like that. I started getting a greater proportion of small fragment peaks when I lowered the reaction volume to 5ul and used 2.5 ul of transposase and 2.5 ul TD. You will have to resuspend your lysed cells in the tagmentation mix. Skip the cleanup step after tagmentation. This method came from the original ATACseq paper for lower cell numbers. Hope that helps.
    Last edited by rbd; 04-02-2015, 08:24 AM.

    Comment


    • #3
      ATAC-seq and bioanalyzer

      Hi,
      I have a 'side question'- In which Bioanalyzer (and kit) did you use? I suppose you used a kit suitable for DNA library with long fragments (>1Kb)..
      Thanks

      Comment


      • #4
        Originally posted by Tal Golan View Post
        Hi,
        I have a 'side question'- In which Bioanalyzer (and kit) did you use? I suppose you used a kit suitable for DNA library with long fragments (>1Kb)..
        Thanks
        Its the Agilent 2100 Bioanalyzer using the High Sensitivity DNA kit. Its intended for fragments under 1KB but the upper marker is at 10KB so you can see some of the larger fragments as well.

        Comment


        • #5
          how many cells you used in the reaction?


          Originally posted by rbd View Post
          I have been using ES cells and for a while I was getting profiles like that. I started getting a greater proportion of small fragment peaks when I lowered the reaction volume to 5ul and used 2.5 ul of transposase and 2.5 ul TD. You will have to resuspend your lysed cells in the tagmentation mix. Skip the cleanup step after tagmentation. This method came from the original ATACseq paper for lower cell numbers. Hope that helps.

          Comment


          • #6
            Perhaphs increasing tagmentation time would help you.... also make sure the cell counts are correct

            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
            17 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-04-2024, 09:00 AM
            0 responses
            48 views
            0 likes
            Last Post seqadmin  
            Working...
            X