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. 2011 Oct 12;6(10):e25842. doi: 10.1371/journal.pone.0025842

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Schrider et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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This graph was generated by randomly adding an individual's genomic sequence data to the total dataset and counting the number of RDD sites eliminated (i.e. found to match genomic sequence) once that individual was added. This was repeated 1,000 times and the average number of eliminated RDDs was calculated for each number of individuals. The value for zero individuals is 929 because this is the total number of RDDs that can be eliminated solely by examining the reference genome.