Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • moriah
    Member
    • Dec 2010
    • 23

    #1

    miRNA proportion in mir-seq

    Hi All,

    I received an Illumina HiSeq output on human mirna-seq and after trimming the adapters and alignment to the genome I realized that only 30% of my reads align to miRNAs while other 70% are tRNA,rRNA and other small RNAs.

    I was wondering whether this miRNA proportion is normal?

    Thanks!
  • Nicolas
    Member
    • Apr 2009
    • 41

    #2
    Hi,

    Did you collapse identical sequences (you should not...)? How did you size-selected your RNA? Which tissues is it from (piRNA are abundant in the germline)?

    Comment

    • moriah
      Member
      • Dec 2010
      • 23

      #3
      No, I didn't collapse and it is from breast tissue (tumor and normal).

      Size selection? What do you mean?
      If you mean the library preparation from total RNA, I don't know.

      Thanks!

      Comment

      • Nicolas
        Member
        • Apr 2009
        • 41

        #4
        The protocol for smallRNA-Seq is not the same as for "classical" RNA-Seq, with the aim of purifying the sample from long RNA and enriching for "smallRNA". At one point, we do run a gel and select for the appropriate size (that might be fly-specific, because there is a very abundant 30nt rRNA in Drosophila).

        Other users' input would be useful here!

        Comment

        • moriah
          Member
          • Dec 2010
          • 23

          #5
          Yes, the protocol for small RNA library preparation was followed. The small RNA where isolated for sure and sequenced. But this low proportion of miRNA in my data is what I am not sure about, is it normal? and if not, where can be the problem?

          Thank you

          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
          • 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, 07:41 AM
          0 responses
          12 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-03-2026, 10:13 AM
          0 responses
          28 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-31-2026, 02:55 AM
          0 responses
          39 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...