Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series

Kevin Drenner; Gargi D. Basu; Laurie J. Goodman; Audrey A. Ozols; Janine R. LoBello; Thomas Royce; Michael S. Gordon; Erkut H. Borazanci; Margaux A. Steinbach; Jeffrey Trent; Sunil Sharma

doi:10.18632/oncotarget.28294

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Addendum:

Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series

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Oncotarget. 2022; 13:1174-1174. https://doi.org/10.18632/oncotarget.28294

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Kevin Drenner^1,*, Gargi D. Basu^2,*, Laurie J. Goodman², Audrey A. Ozols², Janine R. LoBello², Thomas Royce², Michael S. Gordon³, Erkut H. Borazanci³, Margaux A. Steinbach³, Jeffrey Trent¹ and Sunil Sharma¹

¹Translational Genomic Research Institute (Tgen), Phoenix, AZ 85004, USA
²Ashion Analytics, LLC, Phoenix, AZ 85004, USA
³HonorHealth Research Institute, Scottsdale, AZ 85258, USA
^*These authors contributed equally to this work

Published: October 20, 2022

Copyright: © 2022 Drenner et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Consent was added to this article: The study, protocol # HRI-0029 is an IRB approved clinical study, WIRB # 20182804, and all patients signed informed consent to participate.

Original article: Oncotarget. 2021; 12:1836–1847. DOI: https://doi.org/10.18632/oncotarget.28046

All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
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Addendum:

Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series