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Unsupervised generative and graph representation learning for modelling cell differentiation.
Bica, Ioana; Andrés-Terré, Helena; Cvejic, Ana; Liò, Pietro.
Afiliación
  • Bica I; Department of Engineering Science, University of Oxford, Oxford, OX1 3PJ, United Kingdom. ioana.bica@eng.ox.ac.uk.
  • Andrés-Terré H; Department of Computer Science and Technology, University of Cambridge, Cambridge, CB3 0FD, United Kingdom. ioana.bica@eng.ox.ac.uk.
  • Cvejic A; The Alan Turing Institute, London, NW1 2DB, United Kingdom. ioana.bica@eng.ox.ac.uk.
  • Liò P; Department of Computer Science and Technology, University of Cambridge, Cambridge, CB3 0FD, United Kingdom. ha376@cam.ac.uk.
Sci Rep ; 10(1): 9790, 2020 06 17.
Article en En | MEDLINE | ID: mdl-32555334
ABSTRACT
Using machine learning techniques to build representations from biomedical data can help us understand the latent biological mechanism of action and lead to important discoveries. Recent developments in single-cell RNA-sequencing protocols have allowed measuring gene expression for individual cells in a population, thus opening up the possibility of finding answers to biomedical questions about cell differentiation. In this paper, we explore unsupervised generative neural methods, based on the variational autoencoder, that can model cell differentiation by building meaningful representations from the high dimensional and complex gene expression data. We use disentanglement methods based on information theory to improve the data representation and achieve better separation of the biological factors of variation in the gene expression data. In addition, we use a graph autoencoder consisting of graph convolutional layers to predict relationships between single-cells. Based on these models, we develop a computational framework that consists of methods for identifying the cell types in the dataset, finding driver genes for the differentiation process and obtaining a better understanding of relationships between cells. We illustrate our methods on datasets from multiple species and also from different sequencing technologies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Diferenciación Celular / Aprendizaje Automático / Modelos Biológicos Tipo de estudio: Evaluation_studies / Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Diferenciación Celular / Aprendizaje Automático / Modelos Biológicos Tipo de estudio: Evaluation_studies / Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido