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sureLDA  

A Novel Multi-Disease Automated Phenotyping Method for the EHR
View on CRAN: Click here


Download and install sureLDA package within the R console
Install from CRAN:
install.packages("sureLDA")

Install from Github:
library("remotes")
install_github("cran/sureLDA")

Install by package version:
library("remotes")
install_version("sureLDA", "0.1.0-1")



Attach the package and use:
library("sureLDA")
Maintained by
Yuri Ahuja
[Scholar Profile | Author Map]
All associated links for this package
First Published: 2020-11-10
Latest Update: 2020-11-10
Description:
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.
How to cite:
Yuri Ahuja (2020). sureLDA: A Novel Multi-Disease Automated Phenotyping Method for the EHR. R package version 0.1.0-1, https://cran.r-project.org/web/packages/sureLDA. Accessed 21 Nov. 2024.
Previous versions and publish date:
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View sureLDA citation profile
Other R packages that sureLDA depends, imports, suggests or enhances
Complete documentation for sureLDA
Functions, R codes and Examples using the sureLDA R package
Some associated functions: simdata . sureLDA-package . sureLDA . 
Some associated R codes: PheNorm.R . RcppExports.R . data.R . package.R . sureLDA.R .  Full sureLDA package functions and examples
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