Model criticism based on likelihood-free inference, with an application to protein network evolution

被引:94
|
作者
Ratmann, Oliver [1 ]
Andrieu, Christophe [2 ]
Wiuf, Carsten [3 ]
Richardson, Sylvia [4 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Epidemiol & Publ Hlth, London W2 1PG, England
[2] Univ Bristol, Dept Math, Bristol BS8 1TW, Avon, England
[3] Univ Aarhus, Bioinformat Res Ctr, DK-8000 Aarhus C, Denmark
[4] Univ London Imperial Coll Sci Technol & Med, Ctr Biostat, London W1 1PG, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 英国工程与自然科学研究理事会;
关键词
Bayesian inference; intractable likelihoods; Markov chain Monte Carlo; Approximate Bayesian Computation; model uncertainty; MONTE-CARLO; IMPACT;
D O I
10.1073/pnas.0807882106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mathematical models are an important tool to explain and comprehend complex phenomena, and unparalleled computational advances enable us to easily explore them without any or little understanding of their global properties. In fact, the likelihood of the data under complex stochastic models is often analytically or numerically intractable in many areas of sciences. This makes it even more important to simultaneously investigate the adequacy of these models-in absolute terms, against the data, rather than relative to the performance of other models-but no such procedure has been formally discussed when the likelihood is intractable. We provide a statistical interpretation to current developments in likelihood-free Bayesian inference that explicitly accounts for discrepancies between the model and the data, termed Approximate Bayesian Computation under model uncertainty (ABC mu). We augment the likelihood of the data with unknown error terms that correspond to freely chosen checking functions, and provide Monte Carlo strategies for sampling from the associated joint posterior distribution without the need of evaluating the likelihood. We discuss the benefit of incorporating model diagnostics within an ABC framework, and demonstrate how this method diagnoses model mismatch and guides model refinement by contrasting three qualitative models of protein network evolution to the protein interaction datasets of Helicobacter pylori and Treponema pallidum. Our results make a number of model deficiencies explicit, and suggest that the T. pallidum network topology is inconsistent with evolution dominated by link turnover or lateral gene transfer alone.
引用
收藏
页码:10576 / 10581
页数:6
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