Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • chelseabird
    Junior Member
    • Jan 2014
    • 1

    #1

    Output not right from mpileup command?

    I am new to bioinformatics and I just starting working on two datasets in an attempt to identify allele-specific expression. I currently am working on Galaxy until I get a new workstation/server access.

    So far I have 2 BAM files, which were mapped with Tophot, that I am working with to call SNPs. I used samtools to sort both files, and tried to run mpileup locally (but got a segmentation fault). When I run mpileup on Galaxy using the unsorted files, I get output files that are approximately 100GB per BAM file. When I look at the data, there seems to be no chromosome information (reads chrM).

    To troubleshoot, I took a small part of one of the BAM files and ran mpileup locally and filtered the output and the data appeared to be what I wanted (ex. chr1 64179067 A A 75 75 25 23 ., II).

    Is a 100GB output file normal? Are there steps that I am missing as far as filtering the BAM prior to mpileup?

    Note the starting BAM files are 6GB and 5GB.

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, 10-22-2026, 11:13 AM
0 responses
23 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
20 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
36 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
42 views
0 reactions
Last Post SEQadmin2  
Working...