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. 2020 Mar 2;10:3795. doi: 10.1038/s41598-020-60704-0

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© The Author(s) 2020

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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Bar graphs of the filter system for determining the clinically relevant variants proposed for embryo selection for each mode of inheritance: (A) filter sets for determining clinically relevant variants classified as either likely pathogenic or pathogenic and (B) filter sets for variants not yet classified but potentially damaging or disease causative. Filters in each row are successively added to the total number of variants remaining.