Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • lcmb
    Junior Member
    • May 2015
    • 6

    #1

    Comparing Merged Seqs to a Reference Seq

    Hello,

    I recently received paired-end reads from an amplicon library I sequenced with Illumina. I used BBMerge to merge the paired-ends and, now, I would like to compare my merged sequences to a reference. My goal is to analyze where the merged sequence may differ from the reference.

    I have tried to write a small Perl program, but I am continually running into problems. I study DNA repair and, essentially, I would like to compare my merged sequences to the reference so that I may better understand repair efficiency.

    Is anyone aware of any programs/scripts that could help me reach my goal of comparing my merges to a reference? They are about 200bp long. Thank you!
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    BBMap.sh (where you got BBMerge from) will do the comparisons/alignments.

    Added: Is your reference 200 bp long?

    Comment

    • lcmb
      Junior Member
      • May 2015
      • 6

      #3
      Originally posted by GenoMax View Post
      BBMap.sh (where you got BBMerge from) will do the comparisons/alignments.

      Added: Is your reference 200 bp long?
      Yes, it is. Thank you, GenoMax! Will BBMap allow me to set any criteria for the alignment? For example, if I did not want any sequences that differ by more than 10% from my reference.

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        Run bbmap.sh on its own to see all the command line options.

        Here are some relevant options

        Post-Filtering Parameters:

        idfilter=0 Independant of minid; sets exact minimum identity
        allowed for alignments to be printed. Range 0 to 1.
        subfilter=-1 Ban alignments with more than this many substitutions.
        insfilter=-1 Ban alignments with more than this many insertions.
        delfilter=-1 Ban alignments with more than this many deletions.
        indelfilter=-1 Ban alignments with more than this many indels.
        editfilter=-1 Ban alignments with more than this many edits.
        inslenfilter=-1 Ban alignments with an insertion longer than this.
        dellenfilter=-1 Ban alignments with a deletion longer than this.
        Last edited by GenoMax; 05-01-2015, 10:37 AM.

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #5
          You could also convert your reads to fasta format (use reformat.sh from BBMap) and then use blat for the alignments.

          Once you identify the reads that align I suppose you want to do a multiple sequence alignment?

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
            by SEQadmin2



            CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

            Despite this, “CRISPR helped turn genome editing from a specialized technique into
            ...
            07-31-2026, 11:01 AM
          • SEQadmin2
            Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
            by SEQadmin2


            Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

            The systematic characterization of the human proteome has
            ...
            07-20-2026, 11:48 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 08-13-2026, 12:22 PM
          0 responses
          25 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-11-2026, 10:35 AM
          0 responses
          21 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-06-2026, 07:41 AM
          0 responses
          36 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-03-2026, 10:13 AM
          0 responses
          51 views
          0 reactions
          Last Post SEQadmin2  
          Working...