Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • buthercup_ch
    Member
    • Apr 2014
    • 41

    #1

    Comparative genomics_35 bacterial strains

    Hi everyone,

    I'm currently dealing with the comparative analysis of the genome sequence of 35 bacterial strains.
    I AM NOT BIOINFORMATICIAN, but a former collaborator in a former project dealing with 7 strains used CD-HIT for clustering the common orthologs, and I was wondering if the same tool could be used to cluster 35 genomes.

    Is there any CD-HIT expert that could help me with this issue? If CD-HIT is not the tool…, any other suggestion?
  • bioBob
    Member
    • Mar 2011
    • 72

    #2
    Hi, it might help to add some detail here. What is the source of your data? NGS? What did you currently have, SNP and INDEL lists or it sounds like you have predicted gene sequences??

    Comment

    • buthercup_ch
      Member
      • Apr 2014
      • 41

      #3
      Hi bioBob, thanks for you interest.
      The only material I have is a set of 35 genomes in .gb format. Obviously the original data were obtained by HTS in Illumina… ?? I don't know any other details. Some one perform the assembly and annotation and I received the .gb files.
      I'm afraid I can't help more than this.
      Last edited by buthercup_ch; 09-05-2014, 05:37 AM.

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
        by SEQadmin2



        CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

        Despite this, “CRISPR helped turn genome editing from a specialized technique into
        ...
        07-31-2026, 11:01 AM
      • SEQadmin2
        Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
        by SEQadmin2


        Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

        The systematic characterization of the human proteome has
        ...
        07-20-2026, 11:48 AM
      • SEQadmin2
        Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
        by SEQadmin2



        Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
        ...
        07-09-2026, 11:10 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Yesterday, 10:13 AM
      0 responses
      14 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-31-2026, 02:55 AM
      0 responses
      29 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-24-2026, 12:17 PM
      0 responses
      23 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-23-2026, 11:41 AM
      0 responses
      21 views
      0 reactions
      Last Post SEQadmin2  
      Working...