Fig. 3From: hsegHMM: hidden Markov model-based allele-specific copy number alteration analysis accounting for hypersegmentationProbability of identification for all the genotype states from 500 simulated datasets based on creating read counts for normal and tumor cells green lines, blue lines, and red lines indicate the probabilities of identification based on the FACETS, hsegHMM-N, and hsegHMM-T models, respectively; Each dataset consists of 4,942 observations of logR and logORBack to article page