Abstract
BackgroundWith the rapid advancement of genomic sequencing techniques, massive production of gene expression data is becoming possible, which prompts the development of precision medicine. Deep learning is a promising approach for phenotype prediction (clinical diagnosis, prognosis, and drug response) based on gene expression profile. Existing deep learning models are usually considered as black-boxes that provide accurate predictions but are not interpretable. However, accuracy and interpretation are both essential for precision medicine. In addition, most models do not integrate the knowledge of the domain. Hence, making deep learning models interpretable for medical applications using prior biological knowledge is the main focus of this paper.ResultsIn this paper, we propose a new self-explainable deep learning model, called Deep GONet, integrating the Gene Ontology into the hierarchical architecture of the neural network. This model is based on a fully-connected architecture constrained by the Gene Ontology annotations, such that each neuron represents a biological function. The experiments on cancer diagnosis datasets demonstrate that Deep GONet is both easily interpretable and highly performant to discriminate cancer and non-cancer samples.ConclusionsOur model provides an explanation to its predictions by identifying the most important neurons and associating them with biological functions, making the model understandable for biologists and physicians.
Highlights
With the rapid advancement of genomic sequencing techniques, massive production of gene expression data is becoming possible, which prompts the development of precision medicine
We propose a new neural network model, Deep GONet, that is self-explainable and embeds the biological knowledge contained in Gene Ontology (GO)
The architecture of Deep GONet Our model takes in the input layer the gene expression profile of a patient and returns in the output layer the prediction of a phenotype of this patient
Summary
With the rapid advancement of genomic sequencing techniques, massive production of gene expression data is becoming possible, which prompts the development of precision medicine. Deep learning is a promising approach for phenotype prediction (clinical diagnosis, prognosis, and drug response) based on gene expression profile. With the rapid advances of data acquisition technologies, collecting large amounts of different-type data (images, ECG, genomics...) becomes simpler in the medical field It inspires a new form of this field, i.e., precision medicine, which takes advantage of these available data to improve profoundly diagnosis, prognosis, or therapeutic decision. Precision medicine has access to detect in advance a disease, such as cancer, anticipate the progression of the disease, and adapt the therapy according to the characteristics of patients Among these data, genomic data and especially gene expression data play a key role in the development of precision medicine. Machine learning has been used on transcriptomic data to construct classifiers predicting phenotypes (diagnosis, prognosis, treatment) [1]. With the increasing production of transcriptomic data, it is highly likely that deep learning will play a major role to solve these problems
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