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HIV 2-LTR experiment design optimization

Clinical trials are necessary in order to develop treatments for diseases; however, they can often be costly, time consuming, and demanding to the patients. This paper summarizes several common methods used for optimal design that can be used to address these issues. In addition, we introduce a nove...

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Detalles Bibliográficos
Autores principales: Cannon, LaMont, Vargas-Garcia, Cesar A., Jagarapu, Aditya, Piovoso, Michael J., Zurakowski, Ryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224063/
https://www.ncbi.nlm.nih.gov/pubmed/30408070
http://dx.doi.org/10.1371/journal.pone.0206700
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author Cannon, LaMont
Vargas-Garcia, Cesar A.
Jagarapu, Aditya
Piovoso, Michael J.
Zurakowski, Ryan
author_facet Cannon, LaMont
Vargas-Garcia, Cesar A.
Jagarapu, Aditya
Piovoso, Michael J.
Zurakowski, Ryan
author_sort Cannon, LaMont
collection PubMed
description Clinical trials are necessary in order to develop treatments for diseases; however, they can often be costly, time consuming, and demanding to the patients. This paper summarizes several common methods used for optimal design that can be used to address these issues. In addition, we introduce a novel method for optimizing experiment designs applied to HIV 2-LTR clinical trials. Our method employs Bayesian techniques to optimize the experiment outcome by maximizing the Expected Kullback-Leibler Divergence (EKLD) between the a priori knowledge of system parameters before the experiment and the a posteriori knowledge of the system parameters after the experiment. We show that our method is robust and performs equally well if not better than traditional optimal experiment design techniques.
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spelling pubmed-62240632018-11-19 HIV 2-LTR experiment design optimization Cannon, LaMont Vargas-Garcia, Cesar A. Jagarapu, Aditya Piovoso, Michael J. Zurakowski, Ryan PLoS One Research Article Clinical trials are necessary in order to develop treatments for diseases; however, they can often be costly, time consuming, and demanding to the patients. This paper summarizes several common methods used for optimal design that can be used to address these issues. In addition, we introduce a novel method for optimizing experiment designs applied to HIV 2-LTR clinical trials. Our method employs Bayesian techniques to optimize the experiment outcome by maximizing the Expected Kullback-Leibler Divergence (EKLD) between the a priori knowledge of system parameters before the experiment and the a posteriori knowledge of the system parameters after the experiment. We show that our method is robust and performs equally well if not better than traditional optimal experiment design techniques. Public Library of Science 2018-11-08 /pmc/articles/PMC6224063/ /pubmed/30408070 http://dx.doi.org/10.1371/journal.pone.0206700 Text en © 2018 Cannon et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Cannon, LaMont
Vargas-Garcia, Cesar A.
Jagarapu, Aditya
Piovoso, Michael J.
Zurakowski, Ryan
HIV 2-LTR experiment design optimization
title HIV 2-LTR experiment design optimization
title_full HIV 2-LTR experiment design optimization
title_fullStr HIV 2-LTR experiment design optimization
title_full_unstemmed HIV 2-LTR experiment design optimization
title_short HIV 2-LTR experiment design optimization
title_sort hiv 2-ltr experiment design optimization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224063/
https://www.ncbi.nlm.nih.gov/pubmed/30408070
http://dx.doi.org/10.1371/journal.pone.0206700
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