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Christine Nardini

Publications and source records attributed to Christine Nardini.

2 recordsLinked to original sources

TOM: a web-based integrated approach for identification of candidate disease genes.

The massive production of biological data by means of highly parallel devices like microarrays for gene expression has paved the way to new possible approaches in molecular genetics. Among them the possibility of inferring biological answers by querying large amounts of expression data. Based on this principle, we present here TOM, a web-based resource for the efficient extraction of candidate genes for hereditary diseases. The service requires the previous knowledge of at least another gene responsible for the disease and the linkage area, or else of two disease associated genetic intervals. The algorithm uses the information stored in public resources, including mapping, expression and functional databases. Given the queries, TOM will select and list one or more candidate genes. This approach allows the geneticist to bypass the costly and time consuming tracing of genetic markers through entire families and might improve the chance of identifying disease genes, particularly for rare diseases. We present here the tool and the results obtained on known benchmark and on hereditary predisposition to familial thyroid cancer. Our algorithm is available at http://www-micrel.deis.unibo.it/~tom/.

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Discovering coherent biclusters from gene expression data using zero-suppressed binary decision diagrams.

The biclustering method can be a very useful analysis tool when some genes have multiple functions and experimental conditions are diverse in gene expression measurement. This is because the biclustering approach, in contrast to the conventional clustering techniques, focuses on finding a subset of the genes and a subset of the experimental conditions that together exhibit coherent behavior. However, the biclustering problem is inherently intractable, and it is often computationally costly to find biclusters with high levels of coherence. In this work, we propose a novel biclustering algorithm that exploits the zero-suppressedbinary decision diagrams (ZBDDs) data structure to cope with the computational challenges. Our method can find all biclusters that satisfy specific input conditions, and it is scalable to practical gene expression data. We also present experimental results confirming the effectiveness of our approach.

Algorithms↗