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Supplementary Figure S2 Whole-genome siCHILD/Haplarithmisis haplotyping and copy number typing outcomes (digynic-triploidy). (A) Shown here are the digynic triploidy profiles for two embryos. The genomic signatures representing genome-wide haplotypes (haplarithms) and copy number states (haplarithms and normalized Log-R plot) were obtained by implementing siCHILD/Haplarithmisis on single blastomeres as previously described (Zamani Estekiet al., 2015;Dimitriadouet al., 2017). (B) Schematic interpretation of the maternal and paternal haplarithm profiles corre- sponding to digynic triploidy. Shown in this example is the profile of one chromosome. In the case of genome-wide digynic triploidy—as in panel A— the distance between the blue and the red lines (e.g. 0.67 for the paternal and 0.33 for the maternal) remain constant along the entire genome.

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1 Section for Nutrition Research, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom..

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This work has been digitalized and published in 2013 by Verlag Zeitschrift für Naturforschung in cooperation with the Max Planck Society for the Advancement of Science under