Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • sanderson83
    Junior Member
    • Mar 2019
    • 3

    #1

    Denovo assembly system resources

    Hi,

    Hope someone can help me out with an IT/Systems question.

    I currently process fastq files using Trinity for assembly and this roughly takes 4 hours per sample. I have noticed that throughout this time CPU use almost 100% whilst RAM usage maxes out at around 70%.

    I am using a standalone workstation with 2 six core processors and 96 Gb RAM. I have access to 5 of these currently and they are all used independently. This is the system I inherited from my predecessor so I am open to change should it increase throughput.

    My question is....

    Would creation of a small beowulf style cluster using four of the workstations, allow increased system resources and perhaps speed up my assembly and processing time.

    I am no overly familiar with the IT infrastructure side of this so any advice would be appreciated.

    Thanks in advance.
  • Bukowski
    Senior Member
    • Jan 2010
    • 388

    #2
    I wouldn't have thought so. You require all the reads to assemble the genome, so splitting this across a cluster, without a shared/distributed memory model, doesn't fit the assembly paradigm which is why most people use a big box with lots of RAM.

    See:

    Comment

    • sanderson83
      Junior Member
      • Mar 2019
      • 3

      #3
      Hi Bukowski,

      Thanks for your reply.

      If we were to cluster the machines and apply a shared/distributed memory model would I likely see an increase in processing speeds due to higher memory/available cores?

      Sorry if this is a naive question but I need to find a way of increasing throughput if at all possible. Appreciate the advice.

      Comment

      • Bukowski
        Senior Member
        • Jan 2010
        • 388

        #4
        It sounds like your best bet is just doing things in an embarrassingly parallel manner which is what you're currently doing. I may have misinterpreted your original request, though but the short answer is no.

        If you build a cluster, you get a job scheduler, and the best thing about that is that you stop having to worry about manually managing the jobs - when one finishes on one machine, it just starts the next one in the queue - that's the benefit for you building a cluster of your machines.

        I also didn't spot you were using Trinity, so I'm going to assume that you're doing transcriptome assemblies - Trinity is already using the resources efficiently in the machine, so the run time you see, is just the run time. Providing it's not maxing out the memory, it matters not a jot if your CPU utilisation is high - all you care about in terms of performance is that it's not swapping out to disk.

        Your process is CPU bound not memory bound. The only benefit you would gain from a cluster with a shared memory architecture doesn't solve your apparent issue, which isn't to do with RAM.

        https://github.com/trinityrnaseq/tri...g-Requirements suggests you need 256GB of RAM in a machine - but I don't know what organism you're working on or how many reads you have in a sample.

        You might want to look at end of run profiling:

        Trinity RNA-Seq de novo transcriptome assembly. Contribute to trinityrnaseq/trinityrnaseq development by creating an account on GitHub.


        This might give you more of an idea where the bottleneck is.

        Comment

        • sanderson83
          Junior Member
          • Mar 2019
          • 3

          #5
          Perfect.

          Thanks for the comprehensive and helpful response. Stops me wasting any more time looking into this.

          Thanks,
          Sanderson.

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
            by SEQadmin2



            Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

            Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
            ...
            Today, 09:55 AM
          • SEQadmin2
            New Genomics Technologies Take Aim at Long-Standing Limits
            by SEQadmin2


            Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

            We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
            ...
            09-28-2026, 10:25 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, Today, 05:39 AM
          0 responses
          10 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, Yesterday, 09:56 AM
          0 responses
          12 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-09-2026, 11:14 AM
          0 responses
          26 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 09-29-2026, 09:51 AM
          0 responses
          77 views
          0 reactions
          Last Post SEQadmin2  
          Working...