laboratoire IBISC, bat. IBGBI, 23 bd de France, Evry, Salle de réunion 3ème étage: comment y aller
Il est possible de garer sa voiture dans le parking souterrain en appelant la loge à partir de la borne d'entrée
Abstract : Minimization of ATL* Models with Respect to Bisimulation   The aim of this work is to provide a general method to minimize the
 size (number of states) of a model M of an ATL* formula. Our approach
 is founded on the notion of alternating bisimulation: given a model M,
 it is transformed in a stepwise manner into a new model M' minimal
 with respect to bisimulation. The method has been implemented and will
 be integrated into the prover TATL, that constructively decides
 satisfiability of an ATL* formula by building a tableau from which,
 when open, models of the input formula can be extracted.
  
The aim of this work is to provide a general method to minimize the
 size (number of states) of a model M of an ATL* formula. Our approach
 is founded on the notion of alternating bisimulation: given a model M,
 it is transformed in a stepwise manner into a new model M' minimal
 with respect to bisimulation. The method has been implemented and will
 be integrated into the prover TATL, that constructively decides
 satisfiability of an ATL* formula by building a tableau from which,
 when open, models of the input formula can be extracted.
 
Abstract :Abduction based drug target discovery using Boolean control network   Network medicine aims at redefining disease at the biological networks
 level in order to provide a better understanding of the causal
 mechanisms at stake during disease progression. Studies in this field
 have shown that behavioral reprogramming observed in complex diseases
 such as Cancer is caused by molecular network rewiring. Currently,
 most computational approaches rely on simulations to relate molecular
 network perturbations to their phenotypic effect. However, few
 computational methods are available for inferring the molecular
 perturbations responsible for an observed phenotype. During this
 presentation, I will, first, introduce Boolean Control Networks that
 constitute a formalism for expressing network rewiring, then, I will
 specify two modalities of dynamical network reprogramming and present
 an abduction-based algorithm enabling the inference of the causal
 perturbations leading to expected dynamical behaviors. Finally, I will
 show an application of this theoretical approach to the inference of
 causal genes in breast cancer and the prediction of new molecular
 targets for drugs.
  
 Network medicine aims at redefining disease at the biological networks
 level in order to provide a better understanding of the causal
 mechanisms at stake during disease progression. Studies in this field
 have shown that behavioral reprogramming observed in complex diseases
 such as Cancer is caused by molecular network rewiring. Currently,
 most computational approaches rely on simulations to relate molecular
 network perturbations to their phenotypic effect. However, few
 computational methods are available for inferring the molecular
 perturbations responsible for an observed phenotype. During this
 presentation, I will, first, introduce Boolean Control Networks that
 constitute a formalism for expressing network rewiring, then, I will
 specify two modalities of dynamical network reprogramming and present
 an abduction-based algorithm enabling the inference of the causal
 perturbations leading to expected dynamical behaviors. Finally, I will
 show an application of this theoretical approach to the inference of
 causal genes in breast cancer and the prediction of new molecular
 targets for drugs.