Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • 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?

  • #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


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

      Comment


      • #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

        • 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
        • seqadmin
          Strategies for Sequencing Challenging Samples
          by seqadmin


          Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
          03-22-2024, 06:39 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, 04-11-2024, 12:08 PM
        0 responses
        30 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 10:19 PM
        0 responses
        32 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 09:21 AM
        0 responses
        28 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-04-2024, 09:00 AM
        0 responses
        53 views
        0 likes
        Last Post seqadmin  
        Working...
        X