MMRF for Proteome Annotation Applied to Human Protein Disease Prediction. Garcia, B., Ledezma, A., & Sanchis., A. In Proceedings of the 20th International Conference on Inductive Logic Programming (ILP 2010)., of Lecture Notes in Artificial Intelligence, pages In Press, June, 2010. abstract bibtex Biological processes where every gene and protein participates is an essential knowledge for designing disease treatments. Nowadays, these annotations are still unknown for many genes and proteins. Since making annotations from in-vivo experiments is costly, computational predictors are needed for different kinds of annotation such as metabolic pathway, interaction network, protein family, tissue, disease and so on. Biological data has an intrinsic relational structure, including genes and proteins, which can be grouped by many criteria. This hinders the possibility of finding good hypotheses when attribute-value representation is used. Hence, we propose the generic Modular Multi-Relational Framework (MMRF) to predict different kinds of gene and protein annotation using Relational Data Mining (RDM). The specific MMRF application to annotate human protein with diseases verifies that group knowledge (mainly protein-protein interaction pairs) improves the prediction, particularly doubling the area under the precision-recall curve.
@INPROCEEDINGS{Garcia2010,
author = {Beatriz Garcia and Agapito Ledezma and Araceli Sanchis.},
title = {MMRF for Proteome Annotation Applied to Human Protein Disease Prediction.},
booktitle = {Proceedings of the 20th International Conference on Inductive Logic
Programming (ILP 2010).},
year = {2010},
series = {Lecture Notes in Artificial Intelligence},
pages = {In Press},
month = {June},
abstract = {Biological processes where every gene and protein participates is
an essential knowledge for designing disease treatments. Nowadays,
these annotations are still unknown for many genes and proteins.
Since making annotations from in-vivo experiments is costly, computational
predictors are needed for different kinds of annotation such as metabolic
pathway, interaction network, protein family, tissue, disease and
so on. Biological data has an intrinsic relational structure, including
genes and proteins, which can be grouped by many criteria. This hinders
the possibility of finding good hypotheses when attribute-value representation
is used. Hence, we propose the generic Modular Multi-Relational Framework
(MMRF) to predict different kinds of gene and protein annotation
using Relational Data Mining (RDM). The specific MMRF application
to annotate human protein with diseases verifies that group knowledge
(mainly protein-protein interaction pairs) improves the prediction,
particularly doubling the area under the precision-recall curve.},
location = {Firenze, Italy}
}
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