Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Petrichor
    Member
    • Apr 2013
    • 10

    #1

    Average insert size from paired end data

    Hi there!

    I am searching for a way to get the average insert size from my data, that was not included.
    The dataset i am using is paired-end Illumina data and I ran BLAST.

    Has someone a clue or an idea how to get the average insert size from my data?
    Is there maybe a simple solution or even a command for this?

    Best regards,
    Petrichor.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    If you use a standard aligner (bowtie, bwa, etc.) on a small chunk of the data, the resulting SAM file will contain insert sizes for all of the mapped reads. You could then just average that with awk or perl or whatever you like.

    Comment

    • swbarnes2
      Senior Member
      • May 2008
      • 910

      #3
      BLAST? On Illumina data? Why didn't you use a short read aligner?

      Comment

      • boetsie
        Senior Member
        • Feb 2010
        • 245

        #4
        You can only use a short-read aligner if you have a reference, as dpryan suggested. Use the paired-end option of the aligner. If you do not have a close reference, make a quick-and-dirty assembly of a subset of your data. Next, align your paired-end reads to the assembly and obtain the insert-size. Third option, probably the quickest, is to ask for the insert size at your sequence provider

        Regards,
        Boetsie

        Comment

        • Petrichor
          Member
          • Apr 2013
          • 10

          #5
          Thanks for the responds!

          Changed to bowtie2 and used some short awk-commands.
          Got some results, hope they will work.

          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...