Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Francy87
    Member
    • May 2013
    • 28

    #1

    mRNA seq analysis

    Hi!
    I just started with metatranscriptome analysis, so I'm sorry to do a stupid or obvious question... I have metatranscriptome data from food fermentations, obtained through HiSeq. I already analysed the 16S data and so I know the microbiota is not very complex. Reading some other posts and some tutorials, I suppose the first thing to do is mapping them to some reference genomes, using software like bowtie... The question is: since I have reads supposed to be from many different microorganisms, is there a way to map them to more than one genome? Or should I need to map my reads to one organism at the time? If yes, then how can I assemble the files from each genome mapping?
    Can someone suggest me a good pipeline to do this kind of analysis?

    Thanks a lot
    Francesca
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    I guess you just reposted this question in a new forum. Since no one has responded so far to your other post I will get the discussion started.

    Are you aware of the MG-RAST? (http://metagenomics.anl.gov/) You could potentially try that for your dataset.

    Another option could be to just use the genomes that you have identified by your 16S analysis and assemble reads that map to those genomes. A significant fraction of reads may end up being in multiple assemblies since there is no way to accurately classify them. If this would be a problem or not would depend on what your ultimate goal is for this analysis.

    Comment

    • Francy87
      Member
      • May 2013
      • 28

      #3
      Yes, I know about MG-RAST... but someone told me it can't work well with low coverage... as I have... So I'm trying to find a different way. Which software do you suggest to use for microbial metatranscriptome assebly?

      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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 08-06-2026, 07:41 AM
      0 responses
      14 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      31 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-31-2026, 02:55 AM
      0 responses
      40 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-24-2026, 12:17 PM
      0 responses
      26 views
      0 reactions
      Last Post SEQadmin2  
      Working...