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  • ocs
    Member
    • May 2011
    • 27

    #1

    IGV reads (grey vs white)

    Hello folks,

    concerning the Integrative Genomics Viewer:
    What is the difference between the white and the grey reads? Some reads in the alignment are all filled with grey and some are outlined with grey but filled with white. I couldn't find any answer in the manual (http://www.broadinstitute.org/softwa.../AlignmentData).

    Thanks in advance,
    best regards,
    Oliver
  • Seq84
    Member
    • Feb 2011
    • 19

    #2
    Hi,
    Reads filled with white have mapping quality score = 0
    best regards,
    Matteo

    Comment

    • ocs
      Member
      • May 2011
      • 27

      #3
      Thanks!
      Does this mean that they are aligned just by desperation?

      Comment

      • nilshomer
        Nils Homer
        • Nov 2008
        • 1283

        #4
        It usually means there are two or more equally likely locations, and so this location was randomly chosen from that set.

        Comment

        • ocs
          Member
          • May 2011
          • 27

          #5
          Hello nilshomer,

          thanks for your answer. Its a bit confusing, I can think of two equally likly locations that both have a great mapping quality but then its set to zero because its ambiguous?

          Comment

          • Jim Robinson
            Member
            • May 2009
            • 75

            #6
            First apologies this was not documented, we'll correct that. I agree its confusing, I think ambiguous mappings should be indicated by a separate score or field, but that's the way it is.

            Jim

            Comment

            • Orr Shomroni
              Member
              • Oct 2011
              • 26

              #7
              Hello everyone,

              To continue on this grey vs. white issue, I have an IGV plot containing 2 reads: 1 long at a certain position, and another slightly shorter which is one position afterwards (i.e. in terms of positions, the small read is contained within the range of the big read). In IGV, the big read is marked white (i.e. can be aligned elsewhere), the small is grey, and the big read has no SNPs/Indels in its edges. The question is, how is it possible that a certain read can be aligned to multiple positions, whereas its subsequence is unique?
              On the same note, which tool determines whether a read can be mapped to multiple locations (i.e. white bar)? Can IGV calculate that itself?
              "Though it may seem that all's been said and done, originality still lives on" - some unoriginal guy who had nothing better to write as his signature

              Comment

              • Jim Robinson
                Member
                • May 2009
                • 75

                #8
                Hi,

                IGV is not making any judgement calls, is is using the mapping quality. It is a convention with at least some aligners (BWA), if not all aligners, that mapping quality == 0 means the read is not uniquely mapped. IGV does not do any calculation. So if you want to take all interpretation out of the picture a "white" read simply means that the mapping quality has been set to zero by the aligner.

                Jim

                Comment

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