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J. M. Sánchez

dblp:65/577 · DBLP profile ↗
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3ranked-venue papers
0as first author
0since 2021 · last 2006
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 2Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
differential variability analysis
0.112006
Algorithm to find gene expression profiles of deregulation and identify families of disease-altered genes · Bioinform. 2006
Bioinformatics and computational biology › genomics › computational genomics
disease gene identification
0.112006
Algorithm to find gene expression profiles of deregulation and identify families of disease-altered genes · Bioinform. 2006
Bioinformatics and computational biology
gene expression analysis
0.112006
Algorithm to find gene expression profiles of deregulation and identify families of disease-altered genes · Bioinform. 2006
YearPublicationVenuePosition
2006 Algorithm to find gene expression profiles of deregulation and identify families of disease-altered genes
abstract
MOTIVATION: Alteration of gene expression often results in up- or down-regulated genes and the most common analysis strategies look for such differentially expressed genes. However, molecular disease mechanisms typically constitute abnormalities in the regulation of genes producing strong alterations in the expression levels. The search for such deregulation states in the genomic expression profiles will help to identify disease-altered genes better. RESULTS: We have developed an algorithm that searches for the genes which present a significant alteration in the variability of their expression profiles, by comparing an altered state with a control state. The algorithm provides groups of genes and assigns a statistical measure of significance to each group of genes selected. The method also includes a prefilter tool to select genes with a threshold of differential expression that can be set by the user ad casum. The method is evaluated using an experimental set of microarrays of human control and cancer samples from patients with acute promyelocytic leukemia.
Carlos Prieto, M. J. Rivas, J. M. Sánchez, Jesús López-Fidalgo, Javier De Las Rivas
Bioinform.3
2000 Multipopulation genetic programming applied to burn diagnosing
abstract
Genetic programming (GP) has proved useful in optimization problems. The way of representing individuals in this methodology is particularly good when we want to construct decision trees. Decision trees are well suited to representing explicit information and relationships among parameters studied. A set of decision trees could make up a decision support system. In this paper we set out a methodology for developing decision support systems as an aid to medical decision making. Above all, we apply it to diagnosing the evolution of a burn, which is a really difficult task even for specialists. A learning classifier system is developed by means of multipopulation genetic programming (MGP). It uses a set of parameters, obtained by specialist doctors, to predict the evolution of a burn according to its initial stages. The system is first trained with a set of parameters and results of evolutions which have been recorded over a set of clinic cases. Once the system is trained, it is useful for deciding how new cases will probably evolve. Thanks to the use of GP, an explicit expression of the input parameter is provided. This explicit expression takes the form of a decision tree which will be incorporated into software tools that help physicians In their everyday work.
Francisco Fernández de Vega, L. M. Roa, Marco Tomassini, J. M. Sánchez
CEC4
2000 Experimental Study of Isolated Multipulation Genetic Programming
Francisco Fernández de Vega, Marco Tomassini, William F. Punch, J. M. Sánchez
GECCO4