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  • gabrielw
    Junior Member
    • Dec 2010
    • 3

    Upload Bam file to custom track UCSC Genome Browser

    I 'm a newbie in mapping stuff, so I'm training mapping 454 reads, first of all I mapped one file that I got in sra database... so I mapped it using bwa, genereted an sam file... I converted to bam....

    but when I try to upload to http://genome.ucsc.edu/cgi-bin/hgCustom , using the browser to upload directly from my PC and click "submit", it says that Can't read file.bam !!!
    Can someone help me ?? I know that there is other way to upload , hosting the file into a link... but I don 't have where to host my file.bam
  • dawe
    Senior Member
    • Apr 2009
    • 258

    #2
    You don't have to upload a bam file. You need to have it visible at a certain ftp or http uri, then add

    track type=bam bigDataUrl=http://link/to/your/bam/file

    just be sure you have indexed the bam file.

    d

    Comment

    • ulz_peter
      Senior Member
      • Feb 2010
      • 219

      #3
      Just in case your BAM file is too large, you could split it and index the splitted parts.

      In case your BAM File is broken: you could check that out using the picard validateSamFile option.

      But in any case: uploading a large BAM file is slow and loading the data over an external http/ftp server certainly would be a good idea. If you only plan to visualize your alignments you could use stanalone visualization prgrams like IGV, Savant or different others. They also can visualize accompanying data if you got them in the right data format. That would save you some time and issues of uploading...

      Comment

      • sdarko
        Member
        • Apr 2009
        • 52

        #4
        I will second the use of IGV from Broad. It's a great tool to locally view alignments.

        Comment

        • gabrielw
          Junior Member
          • Dec 2010
          • 3

          #5
          sorry for the late answer!
          thanks all for your help... I used picard to validatesam to my bam file and thats what happened
          ERROR: Read groups is empty
          WARNING: Record 1, Read name SRR013983.23952, NM tag (nucleotide differences) is missing
          WARNING: Record 2, Read name SRR013983.59880, NM tag (nucleotide differences) is missing
          WARNING: Record 3, Read name SRR013983.22265, NM tag (nucleotide differences) is missing


          and etc.....

          do u know what is happening? thnks

          Comment

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