sureLDA: 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 <doi:10.1093/jamia/ocaa079> for details.

Package details

AuthorYuri Ahuja [aut, cre], Tianxi Cai [aut], PARSE LTD [aut]
MaintainerYuri Ahuja <Yuri_Ahuja@hms.harvard.edu>
LicenseGPL-3
Version0.1.0-1
URL https://github.com/celehs/sureLDA
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:
install.packages("sureLDA")

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sureLDA documentation built on Nov. 10, 2020, 3:48 p.m.