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Temporal Phenotyping using Deep Predictive Clustering of Disease Progression

ICML 2020 · Time series › Causal and generative time series · approach: State-space and latent dynamics forecasting · 28 citations (OpenAlex)

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Measured effects reported in the paper

What was changedWhereMeasuredEffect
Use predictive clustering with outcome-conditioned centroids rather than the strongest listed baselineAC-TPC · UKCFPurity: 0.751$\pm$0.01 -> 0.807$\pm$0.01Helped
Use predictive clustering with outcome-conditioned centroids rather than the strongest listed baselineAC-TPC · UKCFARI: 0.440$\pm$0.02 -> 0.602$\pm$0.01Helped
Use predictive clustering with outcome-conditioned centroids rather than the strongest listed baselineAC-TPC · ADNIPurity: 0.776$\pm$0.05 -> 0.786$\pm$0.03Helped
Use predictive clustering with outcome-conditioned centroids rather than the strongest listed baselineAC-TPC · ADNIAUROC: 0.756$\pm$0.04 -> 0.768$\pm$0.02Helped
Add sample-wise entropy loss to encourage dominant cluster assignments (ablation)AC-TPC · UKCF, 3 comorbiditiesPurity: 0.573$\pm$0.01 -> 0.808$\pm$0.01Helped
Add sample-wise entropy loss to encourage dominant cluster assignments (ablation)AC-TPC · UKCF, 3 comorbiditiesAUROC: 0.500$\pm$0.00 -> 0.852$\pm$0.00Helped
Add embedding separation loss to prevent centroid collapse (ablation)AC-TPC · UKCF, 3 comorbiditiesPurity: 0.795$\pm$0.01 -> 0.808$\pm$0.01Helped
Add embedding separation loss to encourage distinct label distributions (ablation)AC-TPC · UKCF, 3 comorbiditiesActivated clusters: 8.4 -> 8Hurt
Increase possible cluster count K while using β=1.0AC-TPC · UKCFAverage SI: 0.120Mixed

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