Journal
Genome Medicine
Publication Date
11-29-2019
Volume
11
Issue
1
First Page
76
Document Type
Open Access Publication
DOI
10.1186/s13073-019-0687-x
Rights and Permissions
Danos, A.M., Krysiak, K., Barnell, E.K. et al. Standard operating procedure for curation and clinical interpretation of variants in cancer. Genome Med 11, 76 (2019). https://doi.org/10.1186/s13073-019-0687-x This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Recommended Citation
Danos, Arpad M; Krysiak, Kilannin; Barnell, Erica K; Coffman, Adam C; McMichael, Joshua F; Kiwala, Susanna; Spies, Nicholas C; Sheta, Lana M; Pema, Shahil P; Kujan, Lynzey; Clark, Kaitlin A; Wollam, Amber Z; Wagner, Alex H; Griffith, Malachi; Griffith, Obi L; and et al, "Standard operating procedure for curation and clinical interpretation of variants in cancer." Genome Medicine. 11, 1. 76 (2019).
https://digitalcommons.wustl.edu/open_access_pubs/9765
Supplementary Materials, contains supplemental figures and tables outlining curation SOP guidelines illustrated by workflow figures, tables, and screenshots from the CIViC interface.
