Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • SeqVicious
    Member
    • Sep 2011
    • 20

    Good RIN, bad mRNA?

    Hello, I'm preparing some RNA for RNAseq and I submitted my samples to the local sequencing core for quality control on the bioanalyzer. The results came back and my samples have good RIN values, almost all >9. But I can't see a nice bump for the mRNA in which I am interested. I'm not sure if all of the peaks along the electrophoretogram are obscuring the mRNA. Should I trust these samples based on the RIN value alone? I want to proceed to ribosome depletion but I don't want to waste an expensive kit on samples that might not have good mRNA in them.

    The attached is an example of my bioanalyzer results.

    Thanks!
    Attached Files
  • MU Core
    Member
    • Apr 2008
    • 60

    #2
    You won't visualize the mRNA using the standard RNA quality check. The mRNA is a small percentage of the total RNA from the extraction. What is being visualized is the ribosomal RNA which when intact, as in your sample, you infer a similar level of quality to the mRNA in the sample.

    Comment

    • Asaf
      Member
      • Jul 2014
      • 20

      #3
      If you're still skeptic you can always take some of the RNA and PCR your mRNA of interest to make sure it's there. However, you shouldn't worry as MU Core said, there are no peaks for mRNAs in bioAnalyzer.

      Comment

      • kerplunk412
        Senior Member
        • Jun 2012
        • 119

        #4
        mRNA is only 1-3% of total RNA, so as others have said you can't really see it at all in total RNA. Having intact rRNA peaks is basically an indication that you are not seeing significant degradation in your sample, so you can safely assume that your mRNAs are also intact.

        I will also save you some confusion later: after rRNA depletion you have a large peak of tRNA, so you STILL can't see the mRNA. Also, since so much of the rRNA depleted sample is tRNA, you will need to use more rRNA depleted sample vs poly(A) enriched sample for library prep. For example, if your protocol calls for 1 ng of poly(A) RNA, you should probably use at lease 10 ng of rRNA depleted RNA.

        Also, since you are performing rRNA depletion it doesn't matter much if your RNA is somewhat degraded, as long as it isn't very badly degraded. So I think you can confidently proceed with the RNA you have. Good luck!

        Comment

        • SeqVicious
          Member
          • Sep 2011
          • 20

          #5
          Thank you for the responses. I will trust my RNA based on the rRNA peaks and continue on!

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Nine Things a Sample Prep Scientist Thinks About Before Sequencing
            by SEQadmin2


            I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

            Here are nine questions we think about, in roughly the order they matter, before...
            06-18-2026, 07:11 AM
          • SEQadmin2
            From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
            by SEQadmin2


            Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


            The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
            ...
            06-02-2026, 10:05 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, Today, 05:37 AM
          0 responses
          5 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-26-2026, 11:10 AM
          0 responses
          16 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-17-2026, 06:09 AM
          0 responses
          49 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-09-2026, 11:58 AM
          0 responses
          109 views
          0 reactions
          Last Post SEQadmin2  
          Working...