ArticleProceedings of machine learning research2019
Phenotype Inference with Semi-Supervised Mixed Membership Models.
Article in Proceedings of machine learning research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Trends and opportunities in computable clinical phenotyping: A scoping review.Journal of biomedical informatics · 2023Article
- Psychosocial-Behavioral Phenotyping: A Novel Precision Health Approach to Modeling Behavioral, Psychological, and Social Determinants of Health Using Machine Learning.Annals of behavioral medicine : a publication of the Society of Behavioral Medicine · 2022Article
- Probabilistic Machine Learning for Healthcare.Annual review of biomedical data science · 2021Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Disease phenotyping algorithms are designed to sift through clinical data stores to identify patients with specific diseases. Supervised phenotyping methods require significant quantities of expert-labeled data, while unsupervised methods may learn spurious or non-disease phenotypes. To address these limitations, we propose the Semi-Supervised Mixed Membership Model (SS3M) - a probabilistic graphical model for learning disease phenotypes from partially labeled clinical data. We show SS3M can generate interpretable, disease-specific phenotypes which capture the clinical features of the disease concepts specified by the labels provided to the model. Furthermore, SS3M phenotypes demonstrate competitive predictive performance relative to commonly used baselines.
Identifiers
32490377PMC7266114What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.