Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • wayland
    Junior Member
    • Dec 2009
    • 2

    #1

    total rna quality for library construction

    Hi,

    I have a total RNA sample that shows this RNA pattern in bioanalizer

    Click image for larger version

Name:	3VHZ[87[~TS29@@TJG6IVDY.jpg
Views:	1
Size:	39.1 KB
ID:	307641

    the tRNA tatio 28s/18s is 1.3;but not show RIN values on the Agilent Bioanalyzer. other samples like this pattern have low RIN values on the Agilent Bioanalyzer,such as 6.8.

    do you think that quality is ok?

    thanks a lot
  • pmiguel
    Senior Member
    • Aug 2008
    • 2328

    #2
    Looks good.
    If you want to see your RIN score you can check for errors in the error pane. It may be something like the "5S Region Anomaly Threshold" error. Then you can increase the 5S Region Anomaly Threshold from 0.5 to 1 and it should clear the error and give you a RIN score. But the RIN score will be unduly low due to the amount of small RNAs you have. So it is probably not worth the trouble.
    --
    Phillip

    Comment

    • cnicolet
      Member
      • Dec 2008
      • 35

      #3
      Is this plant RNA? You won't get a good RIN from that, but it looks intact.

      Comment

      • pmiguel
        Senior Member
        • Aug 2008
        • 2328

        #4
        Plant RNA per se, will not necessarily give you poor RIN scores. We have a recent set of wheat RNAs submitted that all gave RINs > 9.5.

        I think, other than actual degradation, the factor that will most lower the RIN score is a high concentration of small RNAs. That is typical of some isolation methods -- the Trizol (or other acid phenol) methods allow much higher yields of low molecular weight RNAs. For some applications that is actually good (well, obviously for small RNA projects). But for normal RNAseq experiments it can cause issues.

        But, yes, it is not uncommon for plants to have a bunch of weird peaks (frequently plastid rRNA).

        --
        Phillip

        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
          ...
          Yesterday, 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
        • SEQadmin2
          Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
          by SEQadmin2



          Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
          ...
          07-09-2026, 11:10 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 02:55 AM
        0 responses
        12 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-24-2026, 12:17 PM
        0 responses
        12 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-23-2026, 11:41 AM
        0 responses
        13 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-20-2026, 11:10 AM
        0 responses
        24 views
        0 reactions
        Last Post SEQadmin2  
        Working...