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Distributed transformer for high order epistasis detection in large-scale datasets.
Graça, Miguel; Nobre, Ricardo; Sousa, Leonel; Ilic, Aleksandar.
Afiliación
  • Graça M; INESC-ID, Instituto Superior Técnico, 1000-029, Lisbon, Portugal. miguel.graca@inesc-id.pt.
  • Nobre R; INESC-ID, Instituto Superior Técnico, 1000-029, Lisbon, Portugal.
  • Sousa L; INESC-ID, Instituto Superior Técnico, 1000-029, Lisbon, Portugal.
  • Ilic A; INESC-ID, Instituto Superior Técnico, 1000-029, Lisbon, Portugal.
Sci Rep ; 14(1): 14579, 2024 06 25.
Article en En | MEDLINE | ID: mdl-38918413
ABSTRACT
Understanding the genetic basis of complex diseases is one of the most important challenges in current precision medicine. To this end, Genome-Wide Association Studies aim to correlate Single Nucleotide Polymorphisms (SNPs) to the presence or absence of certain traits. However, these studies do not consider interactions between several SNPs, known as epistasis, which explain most genetic diseases. Analyzing SNP combinations to detect epistasis is a major computational task, due to the enormous search space. A possible solution is to employ deep learning strategies for genomic prediction, but the lack of explainability derived from the black-box nature of neural networks is a challenge yet to be addressed. Herein, a novel, flexible, portable, and scalable framework for network interpretation based on transformers is proposed to tackle any-order epistasis. The results on various epistasis scenarios show that the proposed framework outperforms state-of-the-art methods for explainability, while being scalable to large datasets and portable to various deep learning accelerators. The proposed framework is validated on three WTCCC datasets, identifying SNPs related to genes known in the literature that have direct relationships with the studied diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Epistasis Genética / Estudio de Asociación del Genoma Completo Límite: Humans Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article País de afiliación: Portugal

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Epistasis Genética / Estudio de Asociación del Genoma Completo Límite: Humans Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article País de afiliación: Portugal
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