Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • statsteam
    Member
    • Sep 2009
    • 19

    #1

    TopHat questions

    Hi,

    I have a few general questions.

    I am planning to do the junction mapping using 76bp reads.

    What is the good anchor length to use (I am currently using 5 with a -5 option)?
    Since the reads are long (I used to use 32 bp reads), I am wondering if I can allow more than 3 matches per segment. TopHat currently allows upto 3 mismatches per segment. I initially wanted to set it up with
    --segment-length 76 -- segment-mismatches 4
    but TopHat threw an error saying the number of mismatches is upto 3 per segment. So, I am currently using
    --segment-length 38 --segment-mismatches 2

    Even though my current setting mimics what I wanted to do, it will not be the same as allowing upto 4 mismatches because the 3' end tends to have more sequencing errors.

    Thank you,
    Statsteam
  • colindaven
    Senior Member
    • Oct 2008
    • 417

    #2
    Hi Statsteam,

    I'm new to Tophat but have used Bowtie extensively, which Tophat uses. There is a limit of three mismatches per seed in Bowtie.

    Not sure about your other questions yet.

    Hope that helps

    Colin

    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, 08-06-2026, 07:41 AM
    0 responses
    23 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    38 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-31-2026, 02:55 AM
    0 responses
    43 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-24-2026, 12:17 PM
    0 responses
    26 views
    0 reactions
    Last Post SEQadmin2  
    Working...