Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Bowtie 2 parameters, these should be generous correct?

    I previously ran my fastq file with parameters I can't remember and it gave me ~82% coverage.

    Today (2 months later), I attempted even a less stringent run using

    --local --norc -N1 -L 15

    (i.e. 15 nucleotide seed with one allowable mismatch)

    This only gave me ~35% coverage.

    I have no clue what happened.

  • #2
    That seed length looks far too short. Even bowtie2's "sensitive" mode (--sensitive) uses a seed length of 20. If you have too small a seed, then bowtie2 will find too many false hits (from a matching seed) and give up on extending them. See the "-D" option:



    If you want a less stringent run, it's easier to just use the standard modifier parameters (e.g. '--very-sensitive', or '--very-sensitive-local').

    Comment


    • #3
      Awesome thanks, so then why didn't I get 100% coverage with a 15 seed. How will a 20 seed perform more optimally?

      Comment


      • #4
        Because bowtie2 gives up on a read once there have been too many seed hits that had failed extensions. As I mentioned before, see the "-D" option:

        Comment


        • #5
          Dear gringer, and other users,

          I would like to pick up this question once more. I had a similar question as KnowNothing2, and am not sure, I understand the -D parameter. Would someone explain it a bit more in detail to me?

          Lets say I have a read of 150bp.
          And with L=10 & i=S,1,0.5, I have one 10bp seed every 7bp (=1+0.5*sqrt(150)).

          How does it work from here? Will bowtie2 extend each seed one by one, and if D=15 fail, it gives up, because it seems that all seeds are no good and it takes too long to find the good alignment?

          Any comment is appreciated. Thanks for your help,
          Katrin

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Advancing Precision Medicine for Rare Diseases in Children
            by seqadmin




            Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
            12-16-2024, 07:57 AM
          • seqadmin
            Recent Advances in Sequencing Technologies
            by seqadmin



            Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

            Long-Read Sequencing
            Long-read sequencing has seen remarkable advancements,...
            12-02-2024, 01:49 PM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 12-17-2024, 10:28 AM
          0 responses
          33 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 12-13-2024, 08:24 AM
          0 responses
          49 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 12-12-2024, 07:41 AM
          0 responses
          34 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 12-11-2024, 07:45 AM
          0 responses
          46 views
          0 likes
          Last Post seqadmin  
          Working...
          X