Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • valei
    Member
    • Sep 2010
    • 14

    #1

    How use TopHat in order to map closely related genes?

    Dear all,
    I'm working with RNA-seq paired-end data and I'm using TopHat-BowTie in order to align my reads against the Human reference genome.
    My problem is the following: I' have some reads coming from genes that are duplicated in the genome and they are very similar in terms of sequence, the only difference between them is that the second gene doesn't have the introns (for example this is the case of GLUD and GLUD2, or NACA and NACA2, etc..). When TopHat works with these reads it prefer align with mismatches in the contiguous sequence (GLUD2 or NACA2) instead of splitting the read in two parts and align it in two separated exon without any mismatch (GLUD or NACA).
    Obviously the correct alignment is the second one, I'm sure of this because I got the same mismatches in all the samples that I analyzed.
    How can I overcome this problem?
    Can I use some option or particular parameter? I would like to constrain TopHat to prefer no-mismatch alignments even if they are splitted in two of more segments.
    I hope my question is clear
    Many thanks!

Latest Articles

Collapse

  • SEQadmin2
    16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
    by SEQadmin2




    NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
    Today, 06:46 AM
  • SEQadmin2
    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
    by SEQadmin2



    Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

    Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
    ...
    10-14-2026, 09:55 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 10-28-2026, 09:57 AM
0 responses
22 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-28-2026, 09:51 AM
0 responses
15 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 11:13 AM
0 responses
68 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
48 views
0 reactions
Last Post SEQadmin2  
Working...