Modeling Cumulative Biological Phenomena with Suppes-Bayes Causal Networks
Several diseases related to cell proliferation are characterized by the accumulation of somatic DNA changes, with respect to wild-type conditions. Cancer and HIV are 2 common examples of such diseases, where the mutational load in the cancerous/viral population increases over time. In these cases, s...
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doaj-6ab2f0c76b2d4aa4928450c3ad57100f2020-11-25T03:17:32ZengSAGE PublishingEvolutionary Bioinformatics1176-93432018-07-011410.1177/1176934318785167Modeling Cumulative Biological Phenomena with Suppes-Bayes Causal NetworksDaniele Ramazzotti0Alex Graudenzi1Giulio Caravagna2Marco Antoniotti3Department of Pathology, Stanford University, Stanford, CA, USADepartment of Informatics, Systems and Communication, University of Milano-Bicocca, Milan, ItalySchool of Informatics, University of Edinburgh, Edinburgh, UKDepartment of Informatics, Systems and Communication, University of Milano-Bicocca, Milan, ItalySeveral diseases related to cell proliferation are characterized by the accumulation of somatic DNA changes, with respect to wild-type conditions. Cancer and HIV are 2 common examples of such diseases, where the mutational load in the cancerous/viral population increases over time. In these cases, selective pressures are often observed along with competition, co-operation, and parasitism among distinct cellular clones. Recently, we presented a mathematical framework to model these phenomena, based on a combination of Bayesian inference and Suppes’ theory of probabilistic causation, depicted in graphical structures dubbed Suppes-Bayes Causal Networks (SBCNs). The SBCNs are generative probabilistic graphical models that recapitulate the potential ordering of accumulation of such DNA changes during the progression of the disease. Such models can be inferred from data by exploiting likelihood-based model selection strategies with regularization. In this article, we discuss the theoretical foundations of our approach and we investigate in depth the influence on the model selection task of (1) the poset based on Suppes’ theory and (2) different regularization strategies. Furthermore, we provide an example of application of our framework to HIV genetic data highlighting the valuable insights provided by the inferred SBCNhttps://doi.org/10.1177/1176934318785167 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Daniele Ramazzotti Alex Graudenzi Giulio Caravagna Marco Antoniotti |
spellingShingle |
Daniele Ramazzotti Alex Graudenzi Giulio Caravagna Marco Antoniotti Modeling Cumulative Biological Phenomena with Suppes-Bayes Causal Networks Evolutionary Bioinformatics |
author_facet |
Daniele Ramazzotti Alex Graudenzi Giulio Caravagna Marco Antoniotti |
author_sort |
Daniele Ramazzotti |
title |
Modeling Cumulative Biological Phenomena with Suppes-Bayes Causal Networks |
title_short |
Modeling Cumulative Biological Phenomena with Suppes-Bayes Causal Networks |
title_full |
Modeling Cumulative Biological Phenomena with Suppes-Bayes Causal Networks |
title_fullStr |
Modeling Cumulative Biological Phenomena with Suppes-Bayes Causal Networks |
title_full_unstemmed |
Modeling Cumulative Biological Phenomena with Suppes-Bayes Causal Networks |
title_sort |
modeling cumulative biological phenomena with suppes-bayes causal networks |
publisher |
SAGE Publishing |
series |
Evolutionary Bioinformatics |
issn |
1176-9343 |
publishDate |
2018-07-01 |
description |
Several diseases related to cell proliferation are characterized by the accumulation of somatic DNA changes, with respect to wild-type conditions. Cancer and HIV are 2 common examples of such diseases, where the mutational load in the cancerous/viral population increases over time. In these cases, selective pressures are often observed along with competition, co-operation, and parasitism among distinct cellular clones. Recently, we presented a mathematical framework to model these phenomena, based on a combination of Bayesian inference and Suppes’ theory of probabilistic causation, depicted in graphical structures dubbed Suppes-Bayes Causal Networks (SBCNs). The SBCNs are generative probabilistic graphical models that recapitulate the potential ordering of accumulation of such DNA changes during the progression of the disease. Such models can be inferred from data by exploiting likelihood-based model selection strategies with regularization. In this article, we discuss the theoretical foundations of our approach and we investigate in depth the influence on the model selection task of (1) the poset based on Suppes’ theory and (2) different regularization strategies. Furthermore, we provide an example of application of our framework to HIV genetic data highlighting the valuable insights provided by the inferred SBCN |
url |
https://doi.org/10.1177/1176934318785167 |
work_keys_str_mv |
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