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  • seq_lover
    Member
    • Oct 2011
    • 18

    #1

    BAM Header minor edit

    Hi,

    I have around 20 BAM files and each of them have proper bam header including RG ID, Sample, Library, Platform unit, Description and Platform. I was reading the GATK manual and just realized that the only accepted names for platforms are 454, LS454, Illumina, Solid, ABI_Solid, and CG. But I wanted to be quiet specific when i was converting SAM to BAM and used "Solid5500XL" as the platform name.

    I know there are AddorReplaceReadgroups and ReplaceSamHeader commands in Picard which i can use to edit the BAM header. But it will take some time as I have many large files. Is there an easy way to do so without rewriting the BAM files.

    Thanks in advance.
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    No, you will need to rewrite the BAM files.

    Comment

    • seq_lover
      Member
      • Oct 2011
      • 18

      #3
      Thanks Nils.

      Comment

      • maubp
        Peter (Biopython etc)
        • Jul 2009
        • 1544

        #4
        You could use 'samtools reheader' which will avoid decompressing and recompressing all the read data, but does still have to copy it.

        Comment

        • seq_lover
          Member
          • Oct 2011
          • 18

          #5
          Thanks Peter,

          It was way faster than I predicted.

          Comment

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