Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • jmartin
    Member
    • Dec 2009
    • 78

    #1

    GATK newbie question

    I'm trying to run the GATK Unified Genotyper on a set of bam files that I have coordinate sorted, but when I run the UG its giving me this error message:

    "Input files reads and reference have incompatible contigs: Order of contigs differences, which is unsafe."

    From reading, I believe I need to re-order my reference fasta file to match the order apparent in the coordinate sorted header of my bam files. But I'm not sure how to do that. Is there code somewhere that will let me re-order my reference file to match a given bam file's order?

    I'm using a reference that comprises ~5k small genomes, some of which are in pieces (~188k total sequence records). The file size is 7.3Gb.

    I also think that maybe (probably?) I need to pull out single specific references and run the UG on single references at a time. Its a metagenomic project, and I was hoping to get results for the whole thing at one time, but that might not be realistic. But even if I pull out single, well covered genome references, some of them will be in hundreds of pieces themselves. So I'd still need a way to order my reference. I could probably write up something in perl to do this, but I'm not too strong a coder, and I'm worried that I'd have memory issues trying to hash 188k sequences and juggle them around.

    Can anyone offer me some guidance on this?
  • spreeth84
    Junior Member
    • Jan 2011
    • 9

    #2
    Is this what you are looking for? Picard - Reorder sam
    http://picard.sourceforge.net/comman...tml#ReorderSam

    You can reorder your reads to match the order of your reference sequence.

    Comment

    • jmartin
      Member
      • Dec 2009
      • 78

      #3
      I will take a look at that, thanks for the suggestion. I had thought my alignment sam file needed to be sorted in coordinate order, so I was kind of thinking that I needed to re-order my reference.

      I've been having more luck just extracting single references and working on one at a time though. When I do that the reference fasta is small enough that a simple perl script can order it. I may just give up on trying to call SNPs on my whole subject database in a single go.

      Comment

      • spreeth84
        Junior Member
        • Jan 2011
        • 9

        #4
        The Reordering can be done only after sorting - you will still have to first sort your reads (and reference) by coordinates. Guess that doesn't solve the reference sorting problem you are facing..

        Comment

        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,...
          10-30-2026, 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, Yesterday, 07:59 AM
        0 responses
        13 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 11-05-2026, 09:25 AM
        0 responses
        32 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 11-03-2026, 11:54 AM
        0 responses
        45 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-28-2026, 09:57 AM
        0 responses
        171 views
        0 reactions
        Last Post SEQadmin2  
        Working...