Extended Data Fig. 1: Summary of PGT assays performed.
From: Whole-genome risk prediction of common diseases in human preimplantation embryos
A total of 29 individuals were sequenced on a variety of sequencing platforms. PGT from embryo biopsies were performed by a commercial lab (Natera, formerly Gene Security Network) on the HumanCytoSNP-12 BeadChip array, ranging from 3 to 33 embryos. Coverage and accuracy assessed at genomic positions that are high-confidence genotype calls in parents and born child.
