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. 2016 Jun 1;20(6):276–284. doi: 10.1089/gtmb.2016.0014

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© Silver et al. 2016; Published by Mary Ann Liebert, Inc.

This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

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FIG. 1. — Results of commercial carrier tests and systematic analytics. (A) Donors identified as carriers with each testing panel or methodology are indicated with colored boxes. (B) The proportion of total dysfunctional variants identified as DCV or HLGD by NGS and the subportions detected by the combined commercial carrier testing panels. DCV, defined clinical variants; HLGD, high likelihood of gene dysfunction; NGS, next-generation sequencing. Color images available online at www.liebertpub.com/gtmb