Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • iscancilga
    Junior Member
    • Sep 2018
    • 1

    #1

    Amplicon based sequencing Mutation Calling

    Hi!

    We are investigating the effect of TF-mediated mutations on genome. In the validation part, we narrowed our regions to 1. We sequenced a region and upstream of it and obtained ~100 k coverage with paired end reads. We want to compare mutation frequency between TF-binding and upstream regions. (interested in SNV/small indels).

    I have two questions. One is about mapping and the other is about mutation calling.

    1) Mapping: I use bowtie2 with default conditions. What if my reads are not mapped due to those mutations, so that those reads are discarded ? Shouldn't I decrease the stringency of mapping in mutation calling cases ?

    I used bowtie2 with default settings and obtained %97 mapping.

    2) Mutation calling: I used samtools mpileup —> bcftools call but did not get any mutations in the ranges of our region of interest. I found UNDR ROVER caller that might work for me but any suggestion would be really appreciated.

    TL;DR I am looking for a mutation caller that is focused on targeted region mutations.

    Thank you very much

Latest Articles

Collapse

  • 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
  • SEQadmin2
    New Genomics Technologies Take Aim at Long-Standing Limits
    by SEQadmin2


    Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

    We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
    ...
    09-28-2026, 10:25 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
14 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
21 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-13-2026, 09:56 AM
0 responses
20 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-09-2026, 11:14 AM
0 responses
27 views
0 reactions
Last Post SEQadmin2  
Working...