Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • serenaliao
    Member
    • Jan 2013
    • 22

    #1

    Insert size for overlapped reads?

    When using bismark, if we set -I(min insert size) as 20, will sam file exclude overlapped reads? In my case 70% of pe reads in sam file are overlapped, though I set -I 20.

    Is this normal?
  • chadn737
    Senior Member
    • Jan 2009
    • 392

    #2
    The latest version of bismark uses bowtie2, which has options for dealing with overlapping reads and by default can map mates that overlap. I am not sure if bismark uses the default for this or not, or whether or not this is one of the options available to adjust in Bismark.

    Comment

    • serenaliao
      Member
      • Jan 2013
      • 22

      #3
      Originally posted by chadn737 View Post
      The latest version of bismark uses bowtie2, which has options for dealing with overlapping reads and by default can map mates that overlap. I am not sure if bismark uses the default for this or not, or whether or not this is one of the options available to adjust in Bismark.
      A following question is If I use bismark methylation call extractor for the overlapped pair end reads(count the overlapped CpG twice), will the same reads actually report two CpG calling in the same site?(I want to take advantage of this to check the accuracy of methylation calling)

      Comment

      • dpryan
        Devon Ryan
        • Jul 2011
        • 3478

        #4
        Originally posted by serenaliao View Post
        A following question is If I use bismark methylation call extractor for the overlapped pair end reads(count the overlapped CpG twice), will the same reads actually report two CpG calling in the same site?(I want to take advantage of this to check the accuracy of methylation calling)
        See the --no_overlap option. I recall that, by default, it will report both. With the --no_overlap option, I recall it reporting the call from the first read in a pair. I wrote my own version that checks to see if the calls in overlapping reads are equivalent and found that they differ in ~0.01% of cases in a dataset that I checked. BTW, the accuracy of methylation calls in this case will be purely a function of the sequencing accuracy.

        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, 07-31-2026, 02:55 AM
        0 responses
        18 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-24-2026, 12:17 PM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-23-2026, 11:41 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-20-2026, 11:10 AM
        0 responses
        26 views
        0 reactions
        Last Post SEQadmin2  
        Working...