Journal
Genetics in Medicine
Publication Date
2019
Volume
21
Issue
4
First Page
972
Last Page
981
Document Type
Open Access Publication
DOI
10.1038/s41436-018-0278-z
Rights and Permissions
Barnell EK, Ronning P, Campbell KM, Krysiak K, Ainscough BJ, Sheta LM, Pema SP, Schmidt AD, Richters M, Cotto KC, Danos AM, Ramirez C, Skidmore ZL, Spies NC, Hundal J, Sediqzad MS, Kunisaki J, Gomez F, Trani L, Matlock M, Wagner AH, Swamidass SJ, Griffith M, Griffith OL. Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples. Genet Med. 2019 Apr;21(4):972-981. doi: 10.1038/s41436-018-0278-z. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.
Recommended Citation
Barnell, Erica K.; Ronning, Peter; Campbell, Katie M.; Krysiak, Kilannin; Ainscough, Benjamin J.; Sheta, Lana M.; Pema, Shahil P.; Schmidt, Alina D.; Richters, Megan; Cotto, Kelsy C.; Danos, Arpad M.; Ramirez, Cody; Skidmore, Zachary L.; Spies, Nicholas C.; Hundal, Jasreet; Sediqzad, Malik S.; Kunisaki, Jason; Gomez, Felicia; Trani, Lee; Matlock, Matthew; Wagner, Alex H.; Swamidass, S. Joshua; Griffith, Malachi; and Griffith, Obi L., "Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples." Genetics in Medicine. 21, 4. 972 - 981. (2019).
https://digitalcommons.wustl.edu/open_access_pubs/8247
