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. 2022 Mar 21;28(3):513–516. doi: 10.1038/s41591-022-01735-0

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 1 — 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.