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.
Versions across snapshots
| Version | Repository | File | Size |
|---|---|---|---|
0.1.0-1 |
rolling linux/jammy R-4.5 | sureLDA_0.1.0-1.tar.gz |
125.2 KiB |
0.1.0-1 |
rolling linux/noble R-4.5 | sureLDA_0.1.0-1.tar.gz |
127.0 KiB |
0.1.0-1 |
rolling source/ R- | sureLDA_0.1.0-1.tar.gz |
32.7 KiB |
0.1.0-1 |
latest linux/jammy R-4.5 | sureLDA_0.1.0-1.tar.gz |
125.2 KiB |
0.1.0-1 |
latest linux/noble R-4.5 | sureLDA_0.1.0-1.tar.gz |
127.0 KiB |
0.1.0-1 |
latest source/ R- | sureLDA_0.1.0-1.tar.gz |
32.7 KiB |
0.1.0-1 |
2026-04-26 source/ R- | sureLDA_0.1.0-1.tar.gz |
32.7 KiB |
0.1.0-1 |
2026-04-23 source/ R- | sureLDA_0.1.0-1.tar.gz |
32.7 KiB |
0.1.0-1 |
2026-04-09 windows/windows R-4.5 | sureLDA_0.1.0-1.zip |
448.3 KiB |
0.1.0-1 |
2025-04-20 source/ R- | sureLDA_0.1.0-1.tar.gz |
32.7 KiB |