The Adam optimization method has achieved remarkable success in addressing contemporary challenges in stochastic optimization. This method falls within the realm of adaptive sub-gradient techniques, yet the underlying geometric principles guiding its performance have remained shrouded in mystery, and have long confounded researchers.
We present a systematic Monte Carlo simulation quantifying the statistical power of five common tests for comparing correlated AUROC values under realistic clinical conditions. Evaluating DeLong's test, Hanley-McNeil, bootstrap, permutation testing, and paired CV t-tests across 209 conditions (sample sizes 30-500, AUROC differences 0.
Clinical machine learning papers routinely compare models using AUROC, claiming statistical significance via hypothesis tests. We conducted a comprehensive Monte Carlo simulation evaluating five statistical tests for AUROC comparison—DeLong's test, Hanley-McNeil, bootstrap, permutation, and CV t-test—across 209 conditions spanning sample sizes 30–500, AUROC differences 0.
When the clinical task is unknown a priori, which blood transcriptomic sepsis signature should a clinician deploy? Using nine published signature families across six cross-cohort generalization tasks (2,096 samples, 24 cohorts, SUBSPACE dataset), we show that no individual signature dominates.
Zamora-PCT Score implements a Bayesian bivariate meta-analysis-derived clinical score for differentiating bacterial infection from autoimmune flare in SLE patients. Based on the Zamora/Reitsma bivariate model (k=10 studies, n=604 patients): pooled sensitivity 0.
Zamora-PCT Score implements a Bayesian bivariate meta-analysis-derived clinical score for differentiating bacterial infection from autoimmune flare in SLE patients. Based on the Zamora/Reitsma bivariate model (k=10 studies, n=604 patients): pooled sensitivity 0.
Bayesian sequential monitoring system for lupus nephritis using longitudinal dipstick urinalysis (protein, blood, specific gravity, sediment). Maintains posterior probabilities over 4 disease states (Quiescent/Smoldering/Active_Flare/Nephrotic) using conjugate updating with Markov transition model.
Bayesian sequential monitoring system for lupus nephritis using longitudinal dipstick urinalysis (protein, blood, specific gravity, sediment). Maintains posterior probabilities over 4 disease states (Quiescent/Smoldering/Active_Flare/Nephrotic) using conjugate updating with Markov transition model.
We present VITALS-WATCH, a Bayesian online change-point detection (BOCPD) system for identifying autoimmune flare onset from wearable vital sign data (heart rate, HRV, SpO2). The algorithm implements Adams & MacKay (2007) with multi-channel concordance scoring across three physiological time series.
We present VITALS-WATCH, a Bayesian online change-point detection (BOCPD) system for identifying autoimmune flare onset from wearable vital sign data (heart rate, HRV, SpO2). The algorithm implements Adams & MacKay (2007) with multi-channel concordance scoring across three physiological time series.
Multiple hypothesis testing presents a fundamental challenge in statistical inference: as the number of simultaneous tests increases, so does the probability of false discoveries. This survey provides a comprehensive overview of False Discovery Rate (FDR) control methods, from the seminal Benjamini-Hochberg procedure to modern adaptive and structure-aware algorithms.
Raynaud phenomenon is triggered by cold exposure in >95% of attacks. RAYNAUD-WX models attack probability from ambient temperature, wind chill, humidity, and patient factors (primary vs secondary, calcium channel blocker use, digital ulcer history).
GC-induced bone loss is the most common cause of secondary osteoporosis (Van Staa 2002). OSTEO-GC projects T-score trajectories at 1, 2, and 5 years based on current T-score, daily prednisone dose, duration, and protective factors.
We describe a 10-domain weighted falls risk score for elderly patients with rheumatic diseases, incorporating glucocorticoid-induced myopathy, joint instability, polypharmacy, visual impairment, neuropathy, balance/gait assessment, cognitive function, environmental hazards, prior falls, and disease-specific factors. Domain weights are derived from published falls risk literature (Tinetti 2003, Deandrea 2010, Hayashibara 2010) applied to the rheumatic disease context.