Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Poni
    Junior Member
    • May 2012
    • 7

    #1

    Sequence mapping

    Hi,
    I want to map sequence reads into a reference gene. However, it's possible to have a higher number of SNPs and few insertions and/or deletions for this gene in the genome that I'm analyzing. May I please know which mapping software is suitable for this purpose and whether its useful to allow many mismatches?
    Your advise is highly appreciated.

    Poni
  • TiborNagy
    Senior Member
    • Mar 2010
    • 329

    #2
    I think there is no specific software for this job. Try BWA and decrease the mismatch penalty (-M).

    Comment

    • qiongyi
      Member
      • Nov 2010
      • 10

      #3
      Try BWA or bowtie2.

      Comment

      • Poni
        Junior Member
        • May 2012
        • 7

        #4
        Thanks for the suggestions.
        Poni

        Comment

        • Torst
          Senior Member
          • Apr 2008
          • 275

          #5
          Originally posted by Poni View Post
          Hi,
          I want to map sequence reads into a reference gene. However, it's possible to have a higher number of SNPs and few insertions and/or deletions for this gene in the genome that I'm analyzing. May I please know which mapping software is suitable for this purpose and whether its useful to allow many mismatches?
          Is your reference a whole genome, or just a single gene?

          Nearly all short read aligners trade sensitivity for speed. What you need is increase the sensitivity OR use a true dynamic programming aligner which implements Smith-Waterman or Needleman-Wunsch alignment. Tools which can do this are the FASTA 36 package (http://faculty.virginia.edu/wrpearson/fasta/), Exonerate with the affine model (http://www.ebi.ac.uk/~guy/exonerate/) and Needle/Water (http://emboss.sourceforge.net/).

          Personally, I would use Shrimp 2.x (http://compbio.cs.toronto.edu/shrimp/) which does well with indels.

          Comment

          • Poni
            Junior Member
            • May 2012
            • 7

            #6
            Dear Torst,
            Thanks for this discriptive reply. my reference is a single gene.
            I will try Shrimp 2.x and see.

            Thanks
            Poni

            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
            • SEQadmin2
              Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
              by SEQadmin2



              Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
              ...
              07-09-2026, 11:10 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, Yesterday, 07:41 AM
            0 responses
            12 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            25 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            38 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            25 views
            0 reactions
            Last Post SEQadmin2  
            Working...