Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • empyrean
    Member
    • Sep 2010
    • 52

    #1

    250bp paired end Miseq reads alignment

    Hello all

    Recently we upgraded our miseq and got 2*250 run data. Does anyone have experience in aligning this sort of data? I have been using bwa till now for previous runs when it produced 2*150. Unable use bwa on this data using Bwasw as it didnot support paired end data. I am looking in to bowtie2 now to use as aligner. My references are amplicons and the size is approximately 2kb. In bowtie2, they are suggesting to use bowtie2 for longer genomes. Any thoughts on this?
  • krobison
    Senior Member
    • Nov 2007
    • 734

    #2
    One approach would be to use a tool such as FLASH to merge many of your read pairs into single reads, then align those long reads with bwasw.

    Of course, for what doesn't merge you still have the old problem. But for very long reads, and especially matching to a small target genome (amplicons), I'm wondering if just aligning them independently with bwasw will work just fine. Paired-end alignment is convenient and may give better specificity in some cases, but a large fraction of the time, particularly with a small genome, it isn't actually gaining anything. Of course, you will lose the convenient auto-generation of insert size information, and some sort of post-processing would be needed if you require that.

    Comment

    • JackieBadger
      Senior Member
      • Mar 2009
      • 385

      #3
      you can use Bowtie/Bowtie2...BLAT...BFAST

      Comment

      • swNGS
        Member
        • Nov 2011
        • 83

        #4
        The following paper suggests that bowtie2 offers a marginal advantage over bwasw when it comes to aligning 2x250 versus 2x150. They did use simulated data however, but worth experimenting with.

        Comment

        Latest Articles

        Collapse

        • 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, detection...
          Today, 06:46 AM
        • SEQadmin2
          Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
          by SEQadmin2



          Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

          Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
          ...
          10-14-2026, 09:55 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 10-28-2026, 09:57 AM
        0 responses
        22 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-28-2026, 09:51 AM
        0 responses
        15 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 11:13 AM
        0 responses
        68 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        48 views
        0 reactions
        Last Post SEQadmin2  
        Working...