Fig. 1From: Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlationPercentage of regions with 25-fold coverage per base for each of the 21 known CCRD genes of the panel. The mean and median coverage per gene were 244-fold and 248-fold per base, respectively, with a minimal coverage of 171-fold for RAX2 Back to article page