Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Library insert size

    Hi There,

    I am aiming to sequence bacterial genome with NexteraXT 300bp paired-end reads. I have made my library and all the fragments size (including the adapter) are ranging from 200-650 (I check with the bioanalyzer and gel). Do you think that I will have sufficient insert size in the end? Do you think that I will have good insert size for clustering on the MiSeq platform (using Nextera v3 chemistry)?

    Would be very helpful of your suggestions here!

    Cheers,

    Shimul

  • #2
    Insert sizes will be around 50-500 bp and most of sequenced fragments will be from shorter inserts and their abundance will depend on size distribution of library fragments. Library should cluster and sequence fine but you will not benefit from the long reads. To sequence larger fragments library fragments should be 600-1500 bp.

    Comment


    • #3
      Thanks a lot @ nucacidhunter

      Comment


      • #4
        Originally posted by nucacidhunter View Post
        Insert sizes will be around 50-500 bp and most of sequenced fragments will be from shorter inserts and their abundance will depend on size distribution of library fragments. Library should cluster and sequence fine but you will not benefit from the long reads. To sequence larger fragments library fragments should be 600-1500 bp.
        Hello,

        I am finally running of my sample on the Miseq using MiSeq V3. I have checked the machine now and it shows that after 70 cycles, the >=Q30 is 96%, cluster passing filter 91.4%, and the cluster density is 1092K/mm.

        Do you think that the run is going well?

        Hope to hear back from you soon again!

        Cheers,

        Shimul

        Comment


        • #5
          Originally posted by Shimul View Post
          Hello,

          I am finally running of my sample on the Miseq using MiSeq V3. I have checked the machine now and it shows that after 70 cycles, the >=Q30 is 96%, cluster passing filter 91.4%, and the cluster density is 1092K/mm.

          Do you think that the run is going well?

          Hope to hear back from you soon again!

          Cheers,

          Shimul
          Those numbers are good, so the run is probably going well.
          Josh Kinman

          Comment


          • #6
            jdk787

            Originally posted by jdk787 View Post
            Those numbers are good, so the run is probably going well.
            Thanks a lot Josh!

            Cheers,

            Shimul

            Comment


            • #7
              @Shimul, it is not necessary to post the same question multiple times on the forum. Your run metrics look good.

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