Fig. 3From: Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndromeDesign of the amplicon-based NGS analysis of the coding region of KCNQ1 (based on the sequences of transposase oligos published in Bogdanoff et al. [24]). After the phosphorylation and annealing of the oligo adapters, the adapters bind to the PCR products which are prepared with 3′-A overhangsBack to article page