Alan Schumitzky
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Alan Schumitzky has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Alona Kryshchenko
California State University Channel Islands Camarillo California USA
3 shared publications - Julian Otalvaro
Laboratory of Applied Pharmacokinetics and Bioinformatics, Children’s Hospital of Los Angeles, Los Angeles, United States of America
3 shared publications - Michael Neely
Keck School of Medicine, University of Southern California
3 shared publications - Walter Masami Yamada
Laboratory of Applied Pharmacokinetics and Bioinformatics, Children’s Hospital of Los Angeles, Los Angeles, United States of America
3 shared publications - Rong Chen
Department of Physics Arizona State University 85287 Tempe Arizona USA
2 shared publications - Markus Hovd
Department of Pharmacy University of Oslo Oslo Norway
1 shared publication
Latest Publications
- Open Access
A non-parametric optimal design algorithm for population pharmacokinetics
This paper introduces a non-parametric estimation algorithm designed to effectively estimate the joint distribution of model parameters with application to population pharmacokinetics. Our research group has previously developed the non-parametric adaptive grid (NPAG) algorithm, which while accurate, explores parameter space using an ad-hoc method to suggest new support points. In contrast, the non-parametric optimal design (NPOD) algorithm uses a gradient approach to suggest new support points, which reduces the amount of time spent evaluating non-relevant points and by this the overall number of cycles required to reach convergence. In this paper, we demonstrate that the NPOD algorithm achieves similar solutions to NPAG across two datasets, while being significantly more efficient in both the number of cycles required and overall runtime. Given the importance of developing robust and efficient algorithms for determining drug doses quickly in pharmacokinetics, the NPOD algorithm represents a valuable advancement in non-parametric modeling. Further analysis is needed to determine which algorithm performs better under specific conditions.
Open AccessA non-parametric optimal design algorithm for population pharmacokinetics
This paper introduces a non-parametric estimation algorithm designed to effectively estimate the joint distribution of model parameters with application to population pharmacokinetics. Our research group has previously developed the non-parametric adaptive grid (NPAG) algorithm, which while accurate, explores parameter space using an ad-hoc method to suggest new support points. In contrast, the non-parametric optimal design (NPOD) algorithm uses a gradient approach to suggest new support points, which reduces the amount of time spent evaluating non-relevant points and by this the overall number of cycles required to reach convergence. In this paper, we demonstrate that the NPOD algorithm achieves similar solutions to NPAG across two datasets, while being significantly more efficient in both the number of cycles required and overall runtime. Given the importance of developing robust and efficient algorithms for determining drug doses quickly in pharmacokinetics, the NPOD algorithm represents a valuable advancement in non-parametric modeling. Further analysis is needed to determine which algorithm performs better under specific conditions.
- Open Access
NPSA: Nonparametric Simulated Annealing for Global Optimization
In this paper we describe NPSA, the first parallel nonparametric global maximum likelihood optimization algorithm using simulated annealing (SA). Unlike the nonparametric adaptive grid search method NPAG, which is not guaranteed to find a global optimum solution, and may suffer from the curse of dimensionality, NPSA is a global optimizer and it is free from these grid related issues. We illustrate NPSA by a number of examples including a pharmacokinetics (PK) model for Voriconazole and show that NPSA may be taken as an upgrade to the current grid search based nonparametric methods.
Open AccessNPSA: Nonparametric Simulated Annealing for Global Optimization
In this paper we describe NPSA, the first parallel nonparametric global maximum likelihood optimization algorithm using simulated annealing (SA). Unlike the nonparametric adaptive grid search method NPAG, which is not guaranteed to find a global optimum solution, and may suffer from the curse of dimensionality, NPSA is a global optimizer and it is free from these grid related issues. We illustrate NPSA by a number of examples including a pharmacokinetics (PK) model for Voriconazole and show that NPSA may be taken as an upgrade to the current grid search based nonparametric methods.
- Open Access
RPEM: Randomized Monte Carlo Parametric Expectation Maximization Algorithm
Inspired from quantum Monte Carlo, by using unbiased estimators all the time and sampling discrete and continuous variables at the same time using Metropolis algorithm, we present a novel, fast, and accurate high performance Monte Carlo Parametric Expectation Maximization (MCPEM) algorithm. We named it Randomized Parametric Expectation Maximization (RPEM). In particular, we compared RPEM with Monolix's SAEM and Certara's QRPEM for a realistic two-compartment Voriconazole model with ordinary differential equations (ODEs) and using simulated data. We show that RPEM is 3 to 4 times faster than SAEM and QRPEM, and more accurate than them in reconstructing the population parameters.
Open AccessRPEM: Randomized Monte Carlo Parametric Expectation Maximization Algorithm
Inspired from quantum Monte Carlo, by using unbiased estimators all the time and sampling discrete and continuous variables at the same time using Metropolis algorithm, we present a novel, fast, and accurate high performance Monte Carlo Parametric Expectation Maximization (MCPEM) algorithm. We named it Randomized Parametric Expectation Maximization (RPEM). In particular, we compared RPEM with Monolix's SAEM and Certara's QRPEM for a realistic two-compartment Voriconazole model with ordinary differential equations (ODEs) and using simulated data. We show that RPEM is 3 to 4 times faster than SAEM and QRPEM, and more accurate than them in reconstructing the population parameters.