Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • kevluv93
    Member
    • Jun 2014
    • 10

    #1

    Navigating De-Novo RNA data

    Hey guys, I just finished a de-novo transcriptome assembly with Trinity and Trinotate. These programs produce individual fastq files that will have the transcriptome in one file, the abundance count in another file, gene ontology in another, etc...

    I'm trying to find RNA sequences that we've identified in a previous experiment in these fastq files, but right now I'm stuck just opening them with notepad and using ctrl + f to find my sequences.

    How do you guys navigate RNA data? What programs do you use to search for sequences in de-novo transcriptomes? Right now I have textfiles with all the sequences bunched up next to each other and I need to organize them.

    Also, for anyone with experience with Trinity, with the outputs of Trinotate (gene ontology, abundance count, etc) is there a way I can incorporate these files into my transcriptome so I can find a sequence and have its abundance and ontology displayed next to it? Basically, I don't want to find a gene, then have to open up another file to find the abundance count, then another to find the signal peptide region, you get my point.

    Thanks for the help guys!
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    You can use blat to align RNA sequences from the previous experiments against the transcriptome you have assembled.

    You will need to have access to a unix/linux machine, which I assume you have since you have done trinity analysis already.

    Comment

    • kevluv93
      Member
      • Jun 2014
      • 10

      #3
      I'm actually using Windows. I can find a linux machine and run these programs, but I used Trinity through an XSEDE supercomputer that doesn't have a graphic user interface. If you could suggest things that work on Windows I would much appreciate it, but I'll definitely give blat a try.

      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, 08-13-2026, 12:22 PM
      0 responses
      26 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-11-2026, 10:35 AM
      0 responses
      21 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-06-2026, 07:41 AM
      0 responses
      36 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      51 views
      0 reactions
      Last Post SEQadmin2  
      Working...