Extended Data Fig. 8. Haplotype phasing results on GM12878 nanoNOMe data.
(a) The number of reads that could be phased into maternal or paternal read based on the presence of heterozygous SNV in the read, showing that 65% of reads could be phased. (b) The fractions of the chromosomes that could be phased (the fraction that had > 10x coverage on each allele after phasing) shows on average, 86 % of the genome could be phased.