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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Main Authors: LaMont Cannon, Cesar A Vargas-Garcia, Aditya Jagarapu, Michael J Piovoso, Ryan Zurakowski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6224063?pdf=render
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author LaMont Cannon
Cesar A Vargas-Garcia
Aditya Jagarapu
Michael J Piovoso
Ryan Zurakowski
author_facet LaMont Cannon
Cesar A Vargas-Garcia
Aditya Jagarapu
Michael J Piovoso
Ryan Zurakowski
author_sort LaMont Cannon
collection DOAJ
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 doaj.art-a6e1e383fb5643e882b812bc2c2455d62022-12-22T02:31:12ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011311e020670010.1371/journal.pone.0206700HIV 2-LTR experiment design optimization.LaMont CannonCesar A Vargas-GarciaAditya JagarapuMichael J PiovosoRyan ZurakowskiClinical 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.http://europepmc.org/articles/PMC6224063?pdf=render
spellingShingle LaMont Cannon
Cesar A Vargas-Garcia
Aditya Jagarapu
Michael J Piovoso
Ryan Zurakowski
HIV 2-LTR experiment design optimization.
PLoS ONE
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
url http://europepmc.org/articles/PMC6224063?pdf=render
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AT cesaravargasgarcia hiv2ltrexperimentdesignoptimization
AT adityajagarapu hiv2ltrexperimentdesignoptimization
AT michaeljpiovoso hiv2ltrexperimentdesignoptimization
AT ryanzurakowski hiv2ltrexperimentdesignoptimization