Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Denovo assembly

    Hi, I am new to sequence assembly donot have knowledge on any software program. I am using CLC genome workbench for the denovo assembly and working on assembling bacterial genome that comes from Ion PGM.
    1. I did assembling of bacterial data (300X coverage) using denovo assembly option in CLC and got around 90 contigs for 1.2Mbp genome. How to reduce number of contigs when reference genome is not available. Also I tried making contigs from the contigs obtained from the first assembly. But No significant improvement.
    2. Same data I assembled using reference. It gave me 100% match.

    I think I am missing something during denovo assembly. I use default assembly parameters suggested by the CLC, also I trim the raw sequences for the adopter removal. Any suggestions highly appreciated. Also please suggest me if any online tool available for the assembly which can be used by any biologist who doesnot have software knowledge..

    Thanks
    Thenna

  • #2
    If you have a reference available, then mapping your contigs back to it might give some insight into the nature of the breaks. Some may simply not be crossable using Ion Torrent technology -- large repeats in particular. Some may be missed overlaps; you may be able to identify errors that prevented joining, but since CLC is a black box there probably isn't much more debugging that can be done with that. You can play with the parameters, but I don't have any experience with CLC to suggest which to play with.

    Comment


    • #3
      Consider contacting CLCBio tech support. They are generally very responsive. That may also be the quickest way to get suggestions on different parameters to try for assembly.

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Recent Advances in Sequencing Analysis Tools
        by seqadmin


        The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
        Today, 07:48 AM
      • seqadmin
        Essential Discoveries and Tools in Epitranscriptomics
        by seqadmin




        The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
        04-22-2024, 07:01 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, Today, 07:17 AM
      0 responses
      6 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 05-02-2024, 08:06 AM
      0 responses
      19 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-30-2024, 12:17 PM
      0 responses
      20 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-29-2024, 10:49 AM
      0 responses
      28 views
      0 likes
      Last Post seqadmin  
      Working...
      X