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1.
Stat Med ; 43(12): 2421-2438, 2024 May 30.
Artigo em Inglês | MEDLINE | ID: mdl-38589978

RESUMO

Identifying predictive factors for an outcome of interest via a multivariable analysis is often difficult when the data set is small. Combining data from different medical centers into a single (larger) database would alleviate this problem, but is in practice challenging due to regulatory and logistic problems. Federated learning (FL) is a machine learning approach that aims to construct from local inferences in separate data centers what would have been inferred had the data sets been merged. It seeks to harvest the statistical power of larger data sets without actually creating them. The FL strategy is not always efficient and precise. Therefore, in this paper we refine and implement an alternative Bayesian federated inference (BFI) framework for multicenter data with the same aim as FL. The BFI framework is designed to cope with small data sets by inferring locally not only the optimal parameter values, but also additional features of the posterior parameter distribution, capturing information beyond what is used in FL. BFI has the additional benefit that a single inference cycle across the centers is sufficient, whereas FL needs multiple cycles. We quantify the performance of the proposed methodology on simulated and real life data.


Assuntos
Teorema de Bayes , Modelos Estatísticos , Estudos Multicêntricos como Assunto , Humanos , Aprendizado de Máquina , Simulação por Computador , Interpretação Estatística de Dados , Análise Multivariada
2.
Biostatistics ; 21(2): e131-e147, 2020 04 01.
Artigo em Inglês | MEDLINE | ID: mdl-30380025

RESUMO

Clinical studies where patients are routinely screened for many genomic features are becoming more routine. In principle, this holds the promise of being able to find genomic signatures for a particular disease. In particular, cancer survival is thought to be closely linked to the genomic constitution of the tumor. Discovering such signatures will be useful in the diagnosis of the patient, may be used for treatment decisions and, perhaps, even the development of new treatments. However, genomic data are typically noisy and high-dimensional, not rarely outstripping the number of patients included in the study. Regularized survival models have been proposed to deal with such scenarios. These methods typically induce sparsity by means of a coincidental match of the geometry of the convex likelihood and a (near) non-convex regularizer. The disadvantages of such methods are that they are typically non-invariant to scale changes of the covariates, they struggle with highly correlated covariates, and they have a practical problem of determining the amount of regularization. In this article, we propose an extension of the differential geometric least angle regression method for sparse inference in relative risk regression models. A software implementation of our method is available on github (https://github.com/LuigiAugugliaro/dgcox).


Assuntos
Bioestatística/métodos , Modelos Estatísticos , Medição de Risco/métodos , Análise de Sobrevida , Simulação por Computador , Humanos , Neoplasias/genética , Neoplasias/mortalidade , Análise de Regressão
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