Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • prm36
    Member
    • Mar 2010
    • 16

    #1

    consensus from mpileup

    Hi,

    I am trying to call the consensus sequence from an mpileup file using samtools (specifically the vcf2fq command).

    The consensus fastq file is produced, and looks correct, but during the running of vcf2fast I receive the following error(?) numerous times:


    Argument "MRSA252^I2001121^I.^IA^I.^I28.2^I.^IDP=1;;CI95=1.5,0;FQ=..." isn't numeric in numeric lt (<) at /samtools-0.1.16/bcftools/vcfutils.pl line 503, <> line 1958656.

    Could anyone explain to me what this means, and whether I am doing something wrong?!

    Cheers

    Paul
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    I don't think anything is wrong. It does that at every point where the DP is 1 or 0. The software will fill in N's at those points. Just let it finish, the look at it, it should be alright.

    Comment

    • prm36
      Member
      • Mar 2010
      • 16

      #3
      Thank you!

      Comment

      • prm36
        Member
        • Mar 2010
        • 16

        #4
        Thank you!!

        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
        21 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 10:48 AM
        0 responses
        18 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...