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FGCNSurv: dually fused graph convolutional network for multi-omics survival prediction

MOTIVATION: Survival analysis is an important tool for modeling time-to-event data, e.g. to predict the survival time of patient after a cancer diagnosis or a certain treatment. While deep neural networks work well in standard prediction tasks, it is still unclear how to best utilize these deep mode...

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Detalles Bibliográficos
Autores principales: Wen, Gang, Li, Limin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412406/
https://www.ncbi.nlm.nih.gov/pubmed/37522887
http://dx.doi.org/10.1093/bioinformatics/btad472
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author Wen, Gang
Li, Limin
author_facet Wen, Gang
Li, Limin
author_sort Wen, Gang
collection PubMed
description MOTIVATION: Survival analysis is an important tool for modeling time-to-event data, e.g. to predict the survival time of patient after a cancer diagnosis or a certain treatment. While deep neural networks work well in standard prediction tasks, it is still unclear how to best utilize these deep models in survival analysis due to the difficulty of modeling right censored data, especially for multi-omics data. Although existing methods have shown the advantage of multi-omics integration in survival prediction, it remains challenging to extract complementary information from different omics and improve the prediction accuracy. RESULTS: In this work, we propose a novel multi-omics deep survival prediction approach by dually fused graph convolutional network (GCN) named FGCNSurv. Our FGCNSurv is a complete generative model from multi-omics data to survival outcome of patients, including feature fusion by a factorized bilinear model, graph fusion of multiple graphs, higher-level feature extraction by GCN and survival prediction by a Cox proportional hazard model. The factorized bilinear model enables to capture cross-omics features and quantify complex relations from multi-omics data. By fusing single-omics features and the cross-omics features, and simultaneously fusing multiple graphs from different omics, GCN with the generated dually fused graph could capture higher-level features for computing the survival loss in the Cox-PH model. Comprehensive experimental results on real-world datasets with gene expression and microRNA expression data show that the proposed FGCNSurv method outperforms existing survival prediction methods, and imply its ability to extract complementary information for survival prediction from multi-omics data. AVAILABILITY AND IMPLEMENTATION: The codes are freely available at https://github.com/LiminLi-xjtu/FGCNSurv.
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spelling pubmed-104124062023-08-11 FGCNSurv: dually fused graph convolutional network for multi-omics survival prediction Wen, Gang Li, Limin Bioinformatics Original Paper MOTIVATION: Survival analysis is an important tool for modeling time-to-event data, e.g. to predict the survival time of patient after a cancer diagnosis or a certain treatment. While deep neural networks work well in standard prediction tasks, it is still unclear how to best utilize these deep models in survival analysis due to the difficulty of modeling right censored data, especially for multi-omics data. Although existing methods have shown the advantage of multi-omics integration in survival prediction, it remains challenging to extract complementary information from different omics and improve the prediction accuracy. RESULTS: In this work, we propose a novel multi-omics deep survival prediction approach by dually fused graph convolutional network (GCN) named FGCNSurv. Our FGCNSurv is a complete generative model from multi-omics data to survival outcome of patients, including feature fusion by a factorized bilinear model, graph fusion of multiple graphs, higher-level feature extraction by GCN and survival prediction by a Cox proportional hazard model. The factorized bilinear model enables to capture cross-omics features and quantify complex relations from multi-omics data. By fusing single-omics features and the cross-omics features, and simultaneously fusing multiple graphs from different omics, GCN with the generated dually fused graph could capture higher-level features for computing the survival loss in the Cox-PH model. Comprehensive experimental results on real-world datasets with gene expression and microRNA expression data show that the proposed FGCNSurv method outperforms existing survival prediction methods, and imply its ability to extract complementary information for survival prediction from multi-omics data. AVAILABILITY AND IMPLEMENTATION: The codes are freely available at https://github.com/LiminLi-xjtu/FGCNSurv. Oxford University Press 2023-07-31 /pmc/articles/PMC10412406/ /pubmed/37522887 http://dx.doi.org/10.1093/bioinformatics/btad472 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Wen, Gang
Li, Limin
FGCNSurv: dually fused graph convolutional network for multi-omics survival prediction
title FGCNSurv: dually fused graph convolutional network for multi-omics survival prediction
title_full FGCNSurv: dually fused graph convolutional network for multi-omics survival prediction
title_fullStr FGCNSurv: dually fused graph convolutional network for multi-omics survival prediction
title_full_unstemmed FGCNSurv: dually fused graph convolutional network for multi-omics survival prediction
title_short FGCNSurv: dually fused graph convolutional network for multi-omics survival prediction
title_sort fgcnsurv: dually fused graph convolutional network for multi-omics survival prediction
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412406/
https://www.ncbi.nlm.nih.gov/pubmed/37522887
http://dx.doi.org/10.1093/bioinformatics/btad472
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