Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Genomics101
    Member
    • May 2012
    • 60

    #1

    Best error correction software and methods for de novo assembly of transcriptomes?

    Greetings! It seems like a while (5 years) since this question was asked and I am sure there has been lots of progress on the topic in that time. I have a nice de novo assembly for a transcriptome from 125bp HiSeq paired-end reads and would like to go through and do an extra step of error correction on the assembly. I'm interested to hear what you experiences have been, positive and negative, with error correction software and methods. Many thanks.
  • westerman
    Rick Westerman
    • Jun 2008
    • 1104

    #2
    Post assembly error correction? I am not sure if this is done, at least not on an automated basis. Certainly people will annotated the assembly and perhaps throw away transcripts that do not annotate or annotated poorly. Mapping the reads back to the assembly and making cut-offs based on that has a high chance of throwing away biologically-true assemblies. Correcting the bases themselves seems like something best done pre assembly.

    Comment

    • Brian Bushnell
      Super Moderator
      • Jan 2014
      • 2709

      #3
      There are some tools for this, such as FinisherSC:
      We introduce FinisherSC, which is a repeat-aware and scalable tool for upgrading de-novo assembly using long reads. Experiments with real data suggest that FinisherSC can provide longer and higher quality contigs than existing tools while maintaining high concordance. Availability The tool and data are available and will be maintained at <http://kakitone.github.io/finishingTool/> Contact dntse{at}stanford.edu


      Not sure how that would work on transcriptomes, though.

      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
        ...
        10-14-2026, 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, 10-22-2026, 11:13 AM
      0 responses
      21 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 10:48 AM
      0 responses
      18 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      36 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      42 views
      0 reactions
      Last Post SEQadmin2  
      Working...