Life sciences · Preprint
arXiv · November 6, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Preprint.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Absorption, distribution, metabolism, excretion, and toxicity (ADMET) models often rely on small, heterogeneous datasets, yet their predictions may determine which compounds proceed to experimental testing. Useful evaluations must therefore assess both predictive performance and the quality of reported probabilities or intervals. We ask which common uncertainty-quantification methods perform best on the 22 Therapeutics Data Commons (TDC) ADMET datasets and what this benchmark can resolve. We compare eleven calibrated pipelines using nested five-fold cross-validation across ten chemical partitions and five model seeds. Ensemble Monte Carlo (MC) dropout has the best average rank for TDC performance, Brier score, and 90% interval score. For TDC performance, however, it is not separated from the other ensemble pipelines; for Brier and interval score, LightGBM is also not ruled out as best. LightGBM wins more individual datasets than any other method for TDC performance and Brier score, but performs poorly on several endpoints. Smaller evaluations can identify a different leader and often fail to recover the broader comparison. These results make LightGBM and an ensemble neural model complementary baselines. Comparative claims should be checked across multiple chemical partitions using statistical analyses matched to the question being asked.