967 research outputs found
The Parameter Houlihan: a solution to high-throughput identifiability indeterminacy for brutally ill-posed problems
One way to interject knowledge into clinically impactful forecasting is to
use data assimilation, a nonlinear regression that projects data onto a
mechanistic physiologic model, instead of a set of functions, such as neural
networks. Such regressions have an advantage of being useful with particularly
sparse, non-stationary clinical data. However, physiological models are often
nonlinear and can have many parameters, leading to potential problems with
parameter identifiability, or the ability to find a unique set of parameters
that minimize forecasting error. The identifiability problems can be minimized
or eliminated by reducing the number of parameters estimated, but reducing the
number of estimated parameters also reduces the flexibility of the model and
hence increases forecasting error. We propose a method, the parameter Houlihan,
that combines traditional machine learning techniques with data assimilation,
to select the right set of model parameters to minimize forecasting error while
reducing identifiability problems. The method worked well: the data
assimilation-based glucose forecasts and estimates for our cohort using the
Houlihan-selected parameter sets generally also minimize forecasting errors
compared to other parameter selection methods such as by-hand parameter
selection. Nevertheless, the forecast with the lowest forecast error does not
always accurately represent physiology, but further advancements of the
algorithm provide a path for improving physiologic fidelity as well. Our hope
is that this methodology represents a first step toward combining machine
learning with data assimilation and provides a lower-threshold entry point for
using data assimilation with clinical data by helping select the right
parameters to estimate
Leveraging 3D chemical similarity, target and phenotypic data in the identification of drug-protein and drug-adverse effect associations
Additional file 5: Figure S4. Number of side effects and targets for each drug in the target-phenotype model
The Arden Syntax for Medical Logic Modules
journal articleBiomedical Informatic
Sharing MLM's: An Experiment between Columbia-Presbyterian and LDS Hospital
Conference PaperBiomedical Informatic
Emerging Standards for Medical Logic
Conference PaperBiomedical Informatic
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