ArticleStatistics in biosciences2024
Enhancing Genetic Risk Prediction through Federated Semi-Supervised Transfer Learning with Inaccurate Electronic Health Record Data.
Article in Statistics in biosciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Large-scale genomics data combined with Electronic Health Records (EHRs) illuminate the path towards personalized disease management and enhanced medical interventions. However, the absence of "gold standard" disease labels makes the development of machine learning models a challenging task. Additionally, imbalances in demographic representation within datasets compromise the development of unbiased healthcare solutions. In response to these challenges, we introduce FEderated Semi-Supervised Transfer Learning (FEST) for improving disease risk predictions in underrepresented populations. FEST facilitates the collaborative training of models across various institutions by leveraging both labeled and unlabeled data from diverse subpopulations. It addresses distributional variations across different populations and healthcare institutions by combining density ratio reweighting and model calibration techniques. Federated learning algorithms are developed for training models using only summary-level statistics. We perform simulation studies to assess the efficacy of FEST in comparisons with a few alternative methods. Subsequently, we apply FEST to training a genetic risk prediction model for type 2 diabetes that targets the African-Ancestry population using data from the Massachusetts General Brigham (MGB) Biobank. Both our computational experiments and real-world data application underline the superior performance of FEST over competing methods.
Indexed as
Identifiers
What Socratic 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 Socratic graph.