Single Nucleotide Polymorphism relevance learning with Random Forests for Type 2 diabetes risk prediction Type 2 diabetes Random Forest Feature learning Predictive model Gini importance

The use of artificial intelligence techniques to find out which Single Nucleotide Polymorphisms (SNPs) promote the development of a disease is one of the features of medical research, as such techniques may potentially aid early diagnosis and help in the prescription of preventive measures. In parti...

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Detalles Bibliográficos
Autores: López Ibáñez, Beatriz, Torrent-Fontbona, Ferran, Viñas, Ramon, Fernández-Real Lemos, José Manuel
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2018
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10256/14506
Acceso en línea:http://hdl.handle.net/10256/14506
Access Level:acceso abierto
Palabra clave:Diabetis no-insulinodependent.
Non-insulin-dependent diabetes.
Diàtesi
Disease susceptibility
Intel·ligència artificial -- Aplicacions a la medicina
Artificial intelligence -- Medical applications
Descripción
Sumario:The use of artificial intelligence techniques to find out which Single Nucleotide Polymorphisms (SNPs) promote the development of a disease is one of the features of medical research, as such techniques may potentially aid early diagnosis and help in the prescription of preventive measures. In particular, the aim is to help physicians to identify the relevant SNPs related to Type 2 diabetes, and to build a decision-support tool for risk prediction. Methods: We use the Random Forest (RF) technique in order to search for the most important attributes (SNPs) related to diabetes, giving a weight (degree of importance), ranging between 0 and 1, to each attribute. Support Vector Machines and Logistic Regression have also been used since they are two other machine learning techniques that are well-established in the health community. Their performance has been compared to that achieved by RF. Furthermore, the relevance of the attributes obtained through the use of RF has then been used to perform predictions with k-Nearest Neighbour method weighting attributes in the similarity measure according to the relevance of the attributes with RF. Results: Testing is performed on a set of 677 subjects. RF is able to handle the complexity of features' interactions, overfitting, and unknown attribute values, providing the SNPs' relevance with an up to 0.89 area under the ROC curve in terms of risk prediction. RF outperforms all the other tested machine learning techniques in terms of prediction accuracy, and in terms of the stability of the estimated relevance of the attributes. Conclusions: The Random Forest is a useful method for learning predictive models and the relevance of SNPs without any underlying assumption