Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • CHRYSES
    Member
    • Dec 2009
    • 13

    samtools mpileup unexpected behaviour

    Hi,

    The command below:
    samtools mpileup -ugf 454AllContigs.fasta my.bam | bcftools view -bvcg - > var.raw.bcf


    exits with the following error:

    [mpileup] 2 samples in 1 input files
    <mpileup> Set max per-sample depth to 4000
    [bcf_sync] incorrect number of fields (7 != 5) at 43:101



    Would that mean that the bam file is missing fields? It is created via the standard methods as outlined in the BWA and samtools manuals.

    The alignments are made using bwa bwasw where 454 reads served as query and references.

    The RG fields are created according to the samtools manual.

    The following fields have been set while merging:
    @RG ID:dUMMY1 SM:dUMMY1 LB:454 PL:454
    @RG ID:dUMMY2 SM:dUMMY2 LB:454 PL:454
    (...)


    Does anyone have an idea what the error cause is? If so, please share it here.


    The description 7 != 5 is not helping much to track the reason.

    Thanks,

    Best regards
  • lh3
    Senior Member
    • Feb 2008
    • 686

    #2
    This has not happened for a while. Could you try the latest version from SVN? What if you use "mpileup -I" to disable indel calling. If both fail, do you have a small example for me to try? Thanks.

    Comment

    • CHRYSES
      Member
      • Dec 2009
      • 13

      #3
      Originally posted by lh3 View Post
      This has not happened for a while. Could you try the latest version from SVN? What if you use "mpileup -I" to disable indel calling. If both fail, do you have a small example for me to try? Thanks.
      The proposed solution with "mpileup -I" has indeed avoided the crash+error, but at the same time it renders samtools to a snp caller only. No indels are called.

      I had done an svn checkout of the trunk lately. The version I am using is:

      $ svn info
      Path: .
      URL: https://samtools.svn.sourceforge.net...samtools/trunk
      Repository Root: https://samtools.svn.sourceforge.net/svnroot/samtools
      Repository UUID: fd675618-d7d1-4fc3-a54f-e58cce934862
      Revision: 902
      Node Kind: directory
      Schedule: normal
      Last Changed Author: lh3lh3
      Last Changed Rev: 902
      Last Changed Date: 2011-01-24 03:46:18 +0100 (Mon, 24 Jan 2011)


      The samtools binary shows this:
      $ samtools

      Program: samtools (Tools for alignments in the SAM format)
      Version: 0.1.12-10 (r896)


      Note that I could not use GATK for indel calling in 454 reads so I wanted to give samtools a shot in this, but it seems like it cannot handle it (yet).

      Do you have any suggestions on making the samtools work with this kind of data?

      Thanks.

      Regards

      Comment

      • Seq84
        Member
        • Feb 2011
        • 19

        #4
        The proposed solution with "mpileup -I" has indeed avoided the crash+error, but at the same time it renders samtools to a snp caller only. No indels are called.
        Me too i had the same problem of CHRYSES and i've solved with -I option.

        Why it happens? is a version problem (0.1.12-10 (r896-r862)) or is a problem internal to the .bam file?

        Thanks in advance

        Comment

        • cnoirot
          Junior Member
          • Feb 2012
          • 3

          #5
          I still have a problem with the version 0.1.18 (r982:295)
          The reference base is always set to N but in fasta file it's not the case !
          I can't perform varFilter.
          Do you have ever seen this problem ?

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
            by SEQadmin2



            Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
            ...
            07-09-2026, 11:10 AM
          • SEQadmin2
            Cancer Drug Resistance: The Lingering Barrier to Rising Survival
            by SEQadmin2



            Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

            There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
            07-08-2026, 05:17 AM
          • GATTACAT
            Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
            by GATTACAT
            Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
            07-01-2026, 11:43 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 07-13-2026, 10:26 AM
          0 responses
          20 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-09-2026, 10:04 AM
          0 responses
          32 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-08-2026, 10:08 AM
          0 responses
          20 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-07-2026, 11:05 AM
          0 responses
          34 views
          0 reactions
          Last Post SEQadmin2  
          Working...