Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Flo1000
    Member
    • Sep 2014
    • 12

    #1

    BWA MEM - which reads were mapped by mate-pair rescue?

    Is there a way to tell which reads were mapped by mate rescue?
    I learned that in BWA results there should be a XT:A:M tag in that case, but in my sam files I can't find any XT tags at all...
  • Flo1000
    Member
    • Sep 2014
    • 12

    #2
    For those who are interested: Apparently, there is no way to tell if a read was mapped by mate pair rescue. From the BWA mailing list:

    For bwa-backtrack, rescue is performed after mapping, but for bwa-mem, rescue is tightly integrated with mapping. The hits resulted from rescue and from single-end mapping are mostly indistinguishable.

    Comment

    • Brian Bushnell
      Super Moderator
      • Jan 2014
      • 2709

      #3
      What do you plan to use that information for, anyway?

      Comment

      • Flo1000
        Member
        • Sep 2014
        • 12

        #4
        The authors of this paper suggest that "Simply removing SNVs for which 7% or more of the mapped reads were mate-rescued increased the validation rate [..] without eliminating any TPs". I wanted to give it a try within our pipeline.

        Comment

        • Brian Bushnell
          Super Moderator
          • Jan 2014
          • 2709

          #5
          Assuming that paper was based on bwa-aln rather than bwa-mem, its results should have little bearing on bwa-mem, since they do rescue differently. But you can avoid rescue altogether simply by mapping all the reads as single-ended rather than paired to see if you get better results.

          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
          9 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...