Garyfallos Konstantinoudis  Discrete versus continuous domain models for disease mapping and applications on childhood cancers
22 Novembre  Sala 34 ore 12
The main goals of disease mapping is to calculate disease risk and identify highrisk areas. Such analyses are hampered by the limited geographical resolution of the available data.
Typically data are counts of cases per spatial unit and the most common approach is the BesagYorkMolli ́e model (BYM). Less frequently, exact geocodes are available, allowing modelling a disease as a point process through LogGaussian Cox processes (LGCPs).
The objective of this study is to examine in a simulation the performance of BYM and LGCPs for disease mapping. We simulated data in the Canton of Zurich in Switzerland sampling cases from the true population mimicking the childhood leukaemia incidence (n=334 during 19852015).
We considered 39 different scenarios varying in the risk generating function (stepwise, smooth, flat risk), the size of the highrisk areas (1, 5 and 10km radii), the risk increase within the highrisk areas (2 and 5fold) and the number of cases (n, 5n and 10n). We used the root mean integrated square error (RMISE) to examine the ability of the models to recover the true risk surface and their sensitivity/specificity in identifying highrisk areas. We found that, for larger radii, LGCPs recover the true risk surface with lower error across almost all scenarios (median RMISE: 9.1727.0) compared to the BYM (median RMISE: 9.1235.6). For radii = 1km and flat risk surfaces BYM performs better. In terms of sensitivity and specificity across almost all scenarios the median area under the curve (AUC) for LGCPs was higher (median AUC: 0.811) compared to the BYM (median AUC: 0.650.93).
We applied these methods to childhood leukaemia incidence in the canton of Zurich during 19852015 and identified two highrisk spatially coherent areas. Our findings suggest that there are important gains to be made from the use of LGCP models in spatial epidemiology.

Roberta De Vito (Department of Biostatistics, Brown University)  Multistudy factor analysis for biological data
14 Novembre  Aula XIV (palazzina Tumminelli) ore 12
We introduce a novel class of factor analysis methodologies for the joint analysis of multiple studies. The goal is to separately identify and estimate 1) common factors shared across multiple studies, and 2) studyspecific factors. We develop a fast Expectation ConditionalMaximization algorithm for parameter estimates and we provide a procedure for choosing the common and specific factors.
We present simulations evaluating the performance of the method and we illustrate it by applying it to gene expression data in ovarian cancer and to nutrientbased dietary patterns and the risk of head and neck cancer. In both cases, we clarify the benefits of a joint analysis compared to the standard factor analysis.
Moreover, we generalize the model in a Bayesian framework. We implement it using sparse modeling of highdimensional factor loadings matrices, both common and specific, using the infinite gamma shrinkage prior. We propose a computationally efficient algorithm, based on a traditional Gibbs sampler, to produce the Bayes estimates of the parameters and to select the number of relevant common factors.
We assess the operating characteristics of our method by means of simulation studies, and we present an application to the prediction of the biological signal from four gene expression studies on ovarian cancer.

Daniel K. Sewell (University of Iowa)  An introduction to the statistical analysis of network data
9 e 10 Settembre  Aula VII (ex Castellano) ore 1016 (con pausa)

Simone Russo  L’invalidità previdenziale: studio dell’incidenza della disabilità nella popolazione in età lavorativa e analisi delle determinanti attraverso dati di registro
5 Giugno  Aula Master (Viale Regina Elena 295) ore 10

Enrico Tucci  L’emigrazione dall’Italia attraverso l’integrazione e l’analisi di rilevazioni statistiche e fonti ufficiali
5 Giugno  Aula Master (Viale Regina Elena 295) ore 10

Modellizzazione statistica dei valori estremi
1617 Aprile  Sala 34 ore 1014

OverdispersedPoisson Model in Claims Reserving: Closed Tool for OneYear Volatility in GLM Framework
29 Marzo  Aula V ore 14.15

Assetliability management for occupational pension funds under market and longevity risk: a case study and alternative modelling approaches
22 Marzo  Aula V ore 15
The modelling of institutional ALM problems has a long history in stochastic programming starting in the late 80’s with the first industry developments such as the wellknown Yasuda Kasai model (Ziemba, Turner, Carino et al, 1994) specifically for pension fund management (PF ALM). Due to economic and demographic pressures in most OECD countries and an increasing interest on PF ALM developments by the industry and by policy makers, we witness nowaday a growing demand for R&D projects to the scientific community.
Taking the view of a PF manager, the presentation will develop around the definition of a generic pension fund (PF) assetliability management (ALM) problem and analyse the key underlying methodological implications of:
(i) it's evolution from an early stage multistage stochastic programming (MSP) with recourse to most recent MSP and distributionally robust (DRO) formulations,
(ii) a peculiar and rich risk spectrum including market risk as well as liability risk, such as longevity risk and demographic factors leading to
(iii) valuation or pricing approaches based on incomplete market assumptions and, due to recent International regulation,
(iv) a riskbased capital allocation for longterm solvency.
The above represent fundamental stochastic and mathematical problems of modern financial optimisation. Two possible approaches to DRO are considered, based on a stochastic control framework or by explicitly introducing an uncertainty set for probability measures and formulating the inner DRO problem as a probability distance minimization problem over a given space of measures.
Keywords: assetliability management, multistage stochastic programming, distributional uncertainty, distributionally robust optimization, solvency ratio, liability pricing, longevity risk, capital allocation.

Incertezza e riproducibilità nella ricerca biomedica
22 Febbraio  Sala 34 ore 11

New formulation of the logisticnormal process to analyze trajectory tracking data
28 Gennaio  Sala 34 ore 10.30
Improved communication systems, shrinking battery sizes and the price drop of tracking devices have led to an increasing availability of trajectory tracking data. These data are often analyzed to understand animals behavior using mixturetype model.
In this work, we propose a new model based on the logisticnormal process. Due to a new formalization and the way we specify the core gionalization matrix of the associated multivariate Gaussian process, we show that our model, differently from other proposals, is invariant with respect to the choice of the reference element and of the order ing of the components of the probability vectors. We estimate the model under a Bayesian framework, using an approximation of the Gaussian process needed to avoid impractical computational time.
We perform a simulation study with the aim of showing the ability of the model to retrieve the parameters used to simulate the data. The model is then applied to the real data where a wolf is observed before and after procreation. Results are easy to interpret, showing differences in the two phases.
Joint work with: Enrico Bibbona (Politecnico di Torino), Clara Grazian (Università di Pescara), Sara Mancinelli (università "Sapienza" di Roma)

