Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • fibar
    Member
    • Feb 2013
    • 19

    #1

    MG-RAST - Alignment parameters of their process statistics?

    After analyzing a metagenomic sample with MG-RAST, you go typically to the Metagenome Overview page to see how it performed.

    At sections 'Metagenome Summary' and 'Analysis Flowchart' you have some first numbers that give you and idea of the process. The thing is they are close but do not match completely. For example:
    1) "7,739,035 sequences (48.5%) contain predicted proteins with known functions"
    2) "a total of 7,662,611 predicted protein coding regions"

    What are the differences between these two sections? What alignment parameters are there behind these statistics? I mean, identity (%), minimal length, max E-value.

    Then, at 'Analysis Flowchart', it says:
    "2,812,269 features (84.9% of annotated features) were assigned to functional categories"

    What functional categories? SEED? And should that number match my Subsystems matrix I download based on 60% identity, 15 bp min-length and 10e-05 E-value (default)?

    Cheers!
  • utpal
    Junior Member
    • Feb 2014
    • 3

    #2
    retriveing the taxonomy and phylogeny or relating together.

    how do you retrive the taxonomy and function together from MG-Rast analysed data. to say how to relate one class of anctionbateria function.

    Comment

    • utpal
      Junior Member
      • Feb 2014
      • 3

      #3
      retriveing the taxonomy and phylogeny or relating together.

      how do you retrive the taxonomy and function together from MG-Rast analysed data. to say how to relate one class of anctionbateria function.

      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
      36 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 10:48 AM
      0 responses
      28 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      41 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      45 views
      0 reactions
      Last Post SEQadmin2  
      Working...