Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Sergio.pv
    Member
    • Jul 2013
    • 21

    #1

    Is 30000 reads too low for mapping (miRNAs)

    Hello community,
    I have just received a fastq file of a study i am conducting.
    It had an overall poor quality, and after filetering reads according to quality and size (minQV=17, min length=16), the number of reads decreased from 95428 to 29635. And the quality increase markedly.

    My question is if it would be still possible to use those ~30000 readss fro mapping.


    Best regards and thanks!
    Sergio
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    You can use any number of reads to do the mapping. Whether you are going to get anything useful out of the mapping is the real question.

    What species do you work with and what kind of analysis (counts/discovery) are you looking to do?

    Comment

    • Sergio.pv
      Member
      • Jul 2013
      • 21

      #3
      Hi GenoMax,
      thank you for the quick reply.
      I work with cattle and I would like to do counts analysis.

      Comment

      • AllSeq
        Registered Vendor
        • Oct 2013
        • 138

        #4
        Even with just counting I generally wouldn't recommend less than 1M reads per sample. But I'm curious to hear about other people's guidelines for miRNA-seq
        AllSeq - The Sequencing Marketplace
        [email protected]
        www.AllSeq.com

        Comment

        Latest Articles

        Collapse

        • kinpict.com
          Reply to 16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
          by kinpict.com
          The part about this topic feels surprisingly grounded, and the details on the page is the bit that made me slow down. I’d keep <a href="https://kinpict.com/">ai family photo generator</a> bookmarked for later.
          Today, 06:37 PM
        • SEQadmin2
          16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
          by SEQadmin2





          NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...
          10-30-2026, 06:46 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 11-12-2026, 07:59 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 11-05-2026, 09:25 AM
        0 responses
        35 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 11-03-2026, 11:54 AM
        2 responses
        56 views
        0 reactions
        Last Post kinpict.com  
        Started by SEQadmin2, 10-28-2026, 09:57 AM
        0 responses
        175 views
        0 reactions
        Last Post SEQadmin2  
        Working...