Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Small RNA - Reads too long after trimming

    I have run a batch of small RNA samples on the SOLiD system. Following sequencing, I've trimmed the adapters (in colour space) using CLC Bio.

    The statistics are as follows...

    Reads Trimmed: 98.1%
    Average Length after trim: 33.7bp

    It is the latter figure that is worrying me...just wondering if anyone has experienced this? My expectation was a read average of ~22 and only 15,000reads fit this catergory.

    Cheers

    D

  • #2
    What was the total read count after adapter processing? What % of reads were ~22nt (15000 out of? ) ?

    Depending on the library, we do get a distribution of sizes up to 30 nt, but most of it would be between 20 and 24nt long (i'd say usually between 90 and 95% of processed). I'm not sure about the Solid sRNA sample prep (we use illumina), but perhaps you might need to check if the library was prepared properly.

    Also, we once had very low throughput but turned out that our adapter sequence was wrong (shorter than it should have been), so you might want to check this too.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin




      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
      04-22-2024, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, Yesterday, 08:47 AM
    0 responses
    16 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    60 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    60 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    54 views
    0 likes
    Last Post seqadmin  
    Working...
    X