Cargando…

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

Detalles Bibliográficos
Autores principales: Drenner, Kevin, Basu, Gargi D., Goodman, Laurie J., Ozols, Audrey A., LoBello, Janine R., Royce, Thomas, Gordon, Michael S., Borazanci, Erkut H., Steinbach, Margaux A., Trent, Jeffrey, Sharma, Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584422/
https://www.ncbi.nlm.nih.gov/pubmed/36289011
http://dx.doi.org/10.18632/oncotarget.28294
_version_ 1784813261470826496
author Drenner, Kevin
Basu, Gargi D.
Goodman, Laurie J.
Ozols, Audrey A.
LoBello, Janine R.
Royce, Thomas
Gordon, Michael S.
Borazanci, Erkut H.
Steinbach, Margaux A.
Trent, Jeffrey
Sharma, Sunil
author_facet Drenner, Kevin
Basu, Gargi D.
Goodman, Laurie J.
Ozols, Audrey A.
LoBello, Janine R.
Royce, Thomas
Gordon, Michael S.
Borazanci, Erkut H.
Steinbach, Margaux A.
Trent, Jeffrey
Sharma, Sunil
author_sort Drenner, Kevin
collection PubMed
description
format Online
Article
Text
id pubmed-9584422
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-95844222022-10-21 Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series Drenner, Kevin Basu, Gargi D. Goodman, Laurie J. Ozols, Audrey A. LoBello, Janine R. Royce, Thomas Gordon, Michael S. Borazanci, Erkut H. Steinbach, Margaux A. Trent, Jeffrey Sharma, Sunil Oncotarget Addendum Impact Journals LLC 2022-10-20 /pmc/articles/PMC9584422/ /pubmed/36289011 http://dx.doi.org/10.18632/oncotarget.28294 Text en Copyright: © 2022 Drenner et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Addendum
Drenner, Kevin
Basu, Gargi D.
Goodman, Laurie J.
Ozols, Audrey A.
LoBello, Janine R.
Royce, Thomas
Gordon, Michael S.
Borazanci, Erkut H.
Steinbach, Margaux A.
Trent, Jeffrey
Sharma, Sunil
Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series
title Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series
title_full Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series
title_fullStr Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series
title_full_unstemmed Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series
title_short Addendum: The value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series
title_sort addendum: the value of comprehensive genomic sequencing to maximize the identification of clinically actionable alterations in advanced cancer patients: a case series
topic Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584422/
https://www.ncbi.nlm.nih.gov/pubmed/36289011
http://dx.doi.org/10.18632/oncotarget.28294
work_keys_str_mv AT drennerkevin addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT basugargid addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT goodmanlauriej addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT ozolsaudreya addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT lobellojaniner addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT roycethomas addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT gordonmichaels addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT borazancierkuth addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT steinbachmargauxa addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT trentjeffrey addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries
AT sharmasunil addendumthevalueofcomprehensivegenomicsequencingtomaximizetheidentificationofclinicallyactionablealterationsinadvancedcancerpatientsacaseseries