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❗ This is a read-only mirror of the CRAN R package repository. sureLDA — A Novel Multi-Disease Automated Phenotyping Method for the EHR. Homepage: https://github.com/celehs/sureLDA Report bugs for this package: https://github.com/celehs/sureLDA/issues

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Overview

Surrogate-guided ensemble Latent Dirichlet Allocation (sureLDA) is a label-free multidimensional phenotyping method. It first uses the PheNorm or MAP algorithm to initialize probabilities based on two surrogate features for each target disease, and then leverages these probabilities to guide the LDA topic model to generate phenotype-specific topics. Finally, it combines phenotype-feature counts with surrogates via clustering ensemble to yield final phenotype probabilities.

See Ahuja et al. JAMIA (2020) for details.

Installation

If devtools is not installed, uncomment the code below and install it from CRAN.

# install.packages("devtools")

Run the code below to install sureLDA from GitHub:

devtools::install_github("celehs/sureLDA")

Getting Started

Click HERE to view a demo with a simulated example.

References

Y. Ahuja, D. Zhou, Z. He, J. Sun, V. M. Castro, V. Gainer, S. N. Murphy, C. Hong, T. Cai. sureLDA: A Multi-Disease Automated Phenotyping Method for the Electronic Health Record. J Am Med Inform Assoc (2020); 27(8): 1235-1243

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❗ This is a read-only mirror of the CRAN R package repository. sureLDA — A Novel Multi-Disease Automated Phenotyping Method for the EHR. Homepage: https://github.com/celehs/sureLDA Report bugs for this package: https://github.com/celehs/sureLDA/issues

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