Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 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

  • #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


    • #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


      • #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


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

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Best Practices for Single-Cell Sequencing Analysis
            by seqadmin



            While isolating and preparing single cells for sequencing was historically the bottleneck, recent technological advancements have shifted the challenge to data analysis. This highlights the rapidly evolving nature of single-cell sequencing. The inherent complexity of single-cell analysis has intensified with the surge in data volume and the incorporation of diverse and more complex datasets. This article explores the challenges in analysis, examines common pitfalls, offers...
            Yesterday, 07:15 AM
          • seqadmin
            Latest Developments in Precision Medicine
            by seqadmin



            Technological advances have led to drastic improvements in the field of precision medicine, enabling more personalized approaches to treatment. This article explores four leading groups that are overcoming many of the challenges of genomic profiling and precision medicine through their innovative platforms and technologies.

            Somatic Genomics
            “We have such a tremendous amount of genetic diversity that exists within each of us, and not just between us as individuals,”...
            05-24-2024, 01:16 PM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, Yesterday, 08:18 AM
          0 responses
          11 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, Yesterday, 08:04 AM
          0 responses
          12 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 06-03-2024, 06:55 AM
          0 responses
          13 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 05-30-2024, 03:16 PM
          0 responses
          27 views
          0 likes
          Last Post seqadmin  
          Working...
          X