26,023 research outputs found
PACMAS: A Personalized, Adaptive, and Cooperative MultiAgent System Architecture
In this paper, a generic architecture, designed to
support the implementation of applications aimed at managing
information among different and heterogeneous sources,
is presented. Information is filtered and organized according
to personal interests explicitly stated by the user. User pro-
files are improved and refined throughout time by suitable
adaptation techniques. The overall architecture has been called
PACMAS, being a support for implementing Personalized, Adaptive,
and Cooperative MultiAgent Systems. PACMAS agents are
autonomous and flexible, and can be made personal, adaptive and
cooperative, depending on the given application. The peculiarities
of the architecture are highlighted by illustrating three relevant
case studies focused on giving a support to undergraduate and
graduate students, on predicting protein secondary structure, and
on classifying newspaper articles, respectively
The benefits of in silico modeling to identify possible small-molecule drugs and their off-target interactions
Accepted for publication in a future issue of Future Medicinal Chemistry.The research into the use of small molecules as drugs continues to be a key driver in the development of molecular databases, computer-aided drug design software and collaborative platforms. The evolution of computational approaches is driven by the essential criteria that a drug molecule has to fulfill, from the affinity to targets to minimal side effects while having adequate absorption, distribution, metabolism, and excretion (ADME) properties. A combination of ligand- and structure-based drug development approaches is already used to obtain consensus predictions of small molecule activities and their off-target interactions. Further integration of these methods into easy-to-use workflows informed by systems biology could realize the full potential of available data in the drug discovery and reduce the attrition of drug candidates.Peer reviewe
MASSP3: A System for Predicting Protein Secondary Structure
A system that resorts to multiple experts for dealing with the problem of predicting secondary structures is described, whose performances are comparable to those obtained by other state-of-the-art predictors. The system performs an overall processing based on two main steps: first, a "sequence-to-structure" prediction is performed, by resorting to a population of hybrid genetic-neural experts, and then a "structure-to-structure" prediction is performed, by resorting to a feedforward artificial neural networks. To investigate the performance of the proposed approach, the system has been tested on the RS126 set of proteins. Experimental results (about 76% of accuracy) point to the validity of the approach
Identification of functionally related enzymes by learning-to-rank methods
Enzyme sequences and structures are routinely used in the biological sciences
as queries to search for functionally related enzymes in online databases. To
this end, one usually departs from some notion of similarity, comparing two
enzymes by looking for correspondences in their sequences, structures or
surfaces. For a given query, the search operation results in a ranking of the
enzymes in the database, from very similar to dissimilar enzymes, while
information about the biological function of annotated database enzymes is
ignored.
In this work we show that rankings of that kind can be substantially improved
by applying kernel-based learning algorithms. This approach enables the
detection of statistical dependencies between similarities of the active cleft
and the biological function of annotated enzymes. This is in contrast to
search-based approaches, which do not take annotated training data into
account. Similarity measures based on the active cleft are known to outperform
sequence-based or structure-based measures under certain conditions. We
consider the Enzyme Commission (EC) classification hierarchy for obtaining
annotated enzymes during the training phase. The results of a set of sizeable
experiments indicate a consistent and significant improvement for a set of
similarity measures that exploit information about small cavities in the
surface of enzymes
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