Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • rozitaa
    Member
    • Jun 2013
    • 51

    #1

    Shotgun Metagenomics data analysis

    Hi,

    I am new to shotgun metagenomics analysis. I have a project on the human gut microbiota. I know about MG-rast but I want to analyze my data by my own. I have done the quality checking and removal of host contaminated sequences. Now I want to check the taxonomical and functional profile of data. I have seen others use universal single copy marker genes reference. Where can I download these from?
    And What is the next step.

    Thanks
  • fahmida
    Member
    • Aug 2010
    • 54

    #2
    Originally posted by rozitaa View Post
    Hi,

    I am new to shotgun metagenomics analysis. I have a project on the human gut microbiota. I know about MG-rast but I want to analyze my data by my own. I have done the quality checking and removal of host contaminated sequences. Now I want to check the taxonomical and functional profile of data. I have seen others use universal single copy marker genes reference. Where can I download these from?
    And What is the next step.

    Thanks
    Have a look into:

    and
    The website that supports the mothur software program - one of the most widely used tools for analyzing 16S rRNA gene sequence data. Step inside to learn how to use the software, get help, and join our community!


    Reference to databases:


    This should get you started.

    Comment

    • rozitaa
      Member
      • Jun 2013
      • 51

      #3
      Originally posted by fahmida View Post
      Have a look into:

      and
      The website that supports the mothur software program - one of the most widely used tools for analyzing 16S rRNA gene sequence data. Step inside to learn how to use the software, get help, and join our community!


      Reference to databases:


      This should get you started.
      Hi Thanks for quick answer. I have worked with Qiime before. But I mean shotgun sequencing not 16s rRNA analysis!

      Comment

      • sphil
        Senior Member
        • Apr 2010
        • 192

        #4
        you can use QIIME (even though it is on your own risk, as they state)

        Comment

        • cliffbeall
          Senior Member
          • Jan 2010
          • 144

          #5
          MEGAN might be one way to go, I haven't used it recently but the author seems to actively update it.

          There is a different approach here, too:
          Kraal, L., et al. (2014). "The prevalence of species and strains in the human microbiome: a resource for experimental efforts." PLoS ONE 9(5): e97279.

          Is the marker gene approach you are mentioning MetaPhlan? I don't know much about that.

          Comment

          • bastianwur
            Member
            • Feb 2014
            • 98

            #6
            Cross-assembly, then taxonomic annotation (MEGAN or alike), gene calling, annotation, that should be the savest and easiest way to go.

            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
            22 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...