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...

Full description

Bibliographic Details
Main Authors: Daniele Ramazzotti, Alex Graudenzi, Giulio Caravagna, Marco Antoniotti
Format: Article
Language:English
Published: SAGE Publishing 2018-07-01
Series:Evolutionary Bioinformatics
Online Access:https://doi.org/10.1177/1176934318785167
id doaj-6ab2f0c76b2d4aa4928450c3ad57100f
record_format Article
spelling 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 AT danieleramazzotti modelingcumulativebiologicalphenomenawithsuppesbayescausalnetworks
AT alexgraudenzi modelingcumulativebiologicalphenomenawithsuppesbayescausalnetworks
AT giuliocaravagna modelingcumulativebiologicalphenomenawithsuppesbayescausalnetworks
AT marcoantoniotti modelingcumulativebiologicalphenomenawithsuppesbayescausalnetworks
_version_ 1724631597172391936