pharmacoml is a hybrid AI/ML-assisted covariate screening toolkit for popPK/popPD workflows. It is designed to identify and prioritize likely covariates from EBEs or individual parameters before formal pharmacometric confirmation.
A covariate screening and preselection tool for pharmacometric workflows. It helps narrow the search space before SCM, backward elimination, or final NLME confirmation.
It is not a replacement for NONMEM, nlmixr2, or full population-model validation. Final confirmation still belongs in the pharmacometric model.
The default workflow combines boosting-based discovery, benchmark-backed RFE, AALASSO confirmation, shrinkage-aware logic, optional interaction screening, and an SCM-style bridge.
What users typically run on a new dataset.
from pharmacoml.covselect import HybridScreener
report = HybridScreener(
include_scm=True,
include_interactions=False,
).fit(
ebes=ebes,
covariates=covariates,
parameter_shrinkage={"CL": 0.12, "V": 0.28},
)
report.confirmed_covariates()
report.candidate_covariates()
report.proxy_groups()
| Output | Meaning | Typical use |
|---|---|---|
core_covariates() |
Strongest ML-supported signals | Initial review |
candidate_covariates() |
Practical shortlist to carry forward | SCM/backward elimination input |
confirmed_covariates() |
Compact answer after SCM-style confirmation | Daily-use summary |
proxy_groups() |
Correlated alternatives | Interpretation and de-duplication |
to_nonmem_candidates() |
Export-ready candidate block | Downstream PMx workflow |
pharmacoml is not positioned as a full automated model builder in the current release. It is positioned as a hybrid AI/ML covariate screener: