Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Jetse
    Member
    • Nov 2012
    • 38

    #1

    multiple vcf files to one multisampled vcf file

    Hello everyone,

    Does anyone know how I can create one multisampled vcf file of multiple vcf files? Now I have many vcf files which all contain the SNPs of one sample.

    Does the program bcftools cat create a multisampled bcf file, or does this one only combine the bcf files?

    Or do I have to use samtools mpileup again, now with multiple samples in once?
  • xecco
    Junior Member
    • Mar 2010
    • 1

    #2
    Try with vcftools vcfmerge (or the improved htscmd)



    However, if you want a complete sample-specific information on all variant positions, you'll need to re-run mpileup again

    Comment

    • Jetse
      Member
      • Nov 2012
      • 38

      #3
      Thanks!
      This program looks like it does exactly what I want!

      [EDIT]
      I used this program for combining the vcf files, but the output is not good enough.
      We are going to rerun the samtools mpileup, exactly because the reason you mentioned: the sample-specific information on all variant positions
      Last edited by Jetse; 06-28-2013, 03:26 AM. Reason: new insights

      Comment

      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, Yesterday, 11:13 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, Yesterday, 10:48 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      35 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...