Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Sequence bacterial genome and amplicons on the same run

    Hello everyone,

    At the moment we are using Miseq to sequence both bacterial and viral genomes at very low throughput. I would like to know if there could be any problem in sequencing these very different genomes on the same run (5mb vs 5 kb).

    Thanks!

    PD: I meant viral genomes not amplicons

  • #2
    As long as they are roughly the same sheared size, this will work well. Total size of the genome doesn't effect the run quality, you just need to account for it when deciding how much of each genome to pool
    Microbial ecologist, running a sequencing core. I have lots of strong opinions on how to survey communities, pretty sure some are even correct.

    Comment


    • #3
      Hi,

      as long as you index each sample individually this should be no problem.
      Just take care that both libraries end up having a similar fragment size. Smaller libraries cluster preferentially, so if your genomes are at 500 bp and your viromes at 300 bp and you mix them 70/30, your read output would be closer to 50/50.

      Comment


      • #4
        Thanks!

        That was my intention. To shear both genomes to almost the same fragment size and indexing each sample.
        Regarding the proportion of bacterial genomes and viromes, is there any way to predict the outcome?(Number of bacterial genomes and viromes might be different each time)

        Comment


        • #5
          Sure, all you need is your genome sizes and the desired coverage and you can calculate how many % of a run is needed per sample.
          You can check out the Illumina Coverage Calculator for that.

          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
          31 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          32 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          28 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          53 views
          0 likes
          Last Post seqadmin  
          Working...
          X