Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • metheuse
    Member
    • Jan 2013
    • 84

    how to analyze whole genome sequencing data (new genome assembling)?

    This is a project to sequence the whole genome of a species (which has not been sequenced yet), assemble the reads, and use the annotations (from related species) to annotate genes on the new genome.
    I'm new to the data analysis in this field. Could anyone tell me what kind of analysis procedures and the widely-used programs I need to follow and use?
    Thanks.
  • Cofactor Genomics
    Registered Vendor
    • Jan 2010
    • 52

    #2
    What our team has found is that depending on whether you are working with a genome of 5Mb, 100Mb, or 3Gb... you will have very different approaches to the library, sequencing, assembly, and annotation approaches. Can you share a bit more? I'm sure you will get more suggestions.

    Jarret Glasscock
    Cofactor Genomics

    Comment

    • metheuse
      Member
      • Jan 2013
      • 84

      #3
      Originally posted by Cofactor Genomics View Post
      What our team has found is that depending on whether you are working with a genome of 5Mb, 100Mb, or 3Gb... you will have very different approaches to the library, sequencing, assembly, and annotation approaches. Can you share a bit more? I'm sure you will get more suggestions.

      Jarret Glasscock
      Cofactor Genomics
      http://www.cofactorgenomics.com
      Thanks for reply. Yes I should give more information. It's a bivalvia genome, about 3Gb.

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by SEQadmin2


        I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

        Here are nine questions we think about, in roughly the order they matter, before...
        06-18-2026, 07:11 AM
      • SEQadmin2
        From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
        by SEQadmin2


        Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


        The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
        ...
        06-02-2026, 10:05 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      38 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-09-2026, 11:58 AM
      0 responses
      101 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-05-2026, 10:09 AM
      0 responses
      123 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-04-2026, 08:59 AM
      0 responses
      114 views
      0 reactions
      Last Post SEQadmin2  
      Working...