A Novel Multi-Disease Automated Phenotyping Method for the EHR

A statistical learning method to simultaneously predict a range of target phenotypes using codified and natural language processing (NLP)-derived Electronic Health Record (EHR) data. See Ahuja et al (2020) JAMIA for details.


Reference manual

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0.1.0-1 by Yuri Ahuja, a year ago


Report a bug at https://github.com/celehs/sureLDA/issues

Browse source code at https://github.com/cran/sureLDA

Authors: Yuri Ahuja [aut, cre] , Tianxi Cai [aut] , PARSE LTD [aut]

Documentation:   PDF Manual  

GPL-3 license

Imports pROC, glmnet, MAP, Rcpp, foreach, doParallel

Depends on Matrix

Suggests knitr, rmarkdown

Linking to Rcpp, RcppArmadillo

See at CRAN