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An architecture for automated reasoning systems for genome-wide studies

Contributo in Atti di convegno
Data di Pubblicazione:
2009
Abstract:
The massive amounts of data generated by high-throughput experiments makes modern biomedical research a data-intensive discipline, shifting the research methodology from a hypothesis-based approach to a hypothesis-free one. A formal procedure should be defined to properly design a study, understand the outcomes and plan improvements for each task performed during the experiments. Such formal approach needs the identification of a high-level conceptual model of the knowledge discovery process occurring in genome-wide studies: this is what existing computational tools lack. Starting from an epistemological model of the discovery process proposed for diagnostic reasoning, we describe how the design and execution of modern genome-wide studies can be modelled using the same framework. We show the general validity of the model, how it can be instantiated to model typical scenarios of genome-wide Studies, and how we use it to develop tools aimed at building semi-automated reasoning systems.
Tipologia CRIS:
4.1 Contributo in Atti di convegno
Keywords:
Decision support system; Genome-wide studies; Reasoning models; Computer Science (all); Theoretical Computer Science
Elenco autori:
Nuzzo, Angelo; Riva, Alberto; Stefanelli, Mario; Bellazzi, Riccardo
Autori di Ateneo:
BELLAZZI RICCARDO
Link alla scheda completa:
https://iris.unipv.it/handle/11571/1127108
Titolo del libro:
Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
Pubblicato in:
LECTURE NOTES IN COMPUTER SCIENCE
Journal
LECTURE NOTES IN COMPUTER SCIENCE
Series
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