Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Maq mismatch

    Hi,

    I am currently using the match function in maq to align sequence reads to a reference genome. I want to increase the mismatch to 5 or 6 but I notice that the limit is at 3. Is there anyway around this?

    thanks

  • #2
    Originally posted by kylle345 View Post
    Hi,

    I am currently using the match function in maq to align sequence reads to a reference genome. I want to increase the mismatch to 5 or 6 but I notice that the limit is at 3. Is there anyway around this?

    thanks
    You will have to use a different aligner. Aligners like BFAST, BWA, bowtie, etc (bowtie is not for SOLiD) will allow you to up the sensitivity at the expense of speed.

    Comment


    • #3
      hi

      Hey thanks for the reply,

      I am currently using bowtie since it is one of the programs that is used by our institute. I am wondering if this is the correct line to use in order to get up to 5 mismatches. If not then how would I do this?

      bowtie -y --maxbts --best -n 5 -q

      Comment


      • #4
        Originally posted by kylle345 View Post
        Hey thanks for the reply,

        I am currently using bowtie since it is one of the programs that is used by our institute. I am wondering if this is the correct line to use in order to get up to 5 mismatches. If not then how would I do this?

        bowtie -y --maxbts --best -n 5 -q
        Looks like the "-n" option can only range from 0-3.
        Code:
          -n/--seedmms <int> max mismatches in seed (can be 0-3, default: -n 2)
        PM Ben Langmead or post a new thread asking how to do this with bowtie. Alternatively, you can ask your institution to use BFAST, which allows you to a priori tune for sensitivity including indels. Admittedly I am the author for the latter.

        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
        17 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 10:19 PM
        0 responses
        22 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 09:21 AM
        0 responses
        16 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-04-2024, 09:00 AM
        0 responses
        46 views
        0 likes
        Last Post seqadmin  
        Working...
        X