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. 2020 Mar 20;22(3):e16810. doi: 10.2196/16810

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©Benjamin Scott Glicksberg, Shohei Burns, Rob Currie, Ann Griffin, Zhen Jane Wang, David Haussler, Theodore Goldstein, Eric Collisson. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 20.03.2020.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research, is properly cited. The complete bibliographic information, a link to the original publication on http://www.jmir.org/, as well as this copyright and license information must be included.

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Breakdown of Foundation One genomics results for pilot cohort. (A) The breakdown of number of variants reported per patient stratified by their current knowledge status. (B) Breakdown of all variants for patients by effect (left) current knowledge status (right). (C) Distribution of cancer type per patient by primary disease (left) and tissue of origin (right). (D) Distribution of genes based on the current knowledge status of encompassed variants. (E) List of the most commonly recurrently mutated genes (N>1) by number of encompassed variants by status. Black dots represent number of unique patients with a variant in the gene.