2012
DOI: 10.1371/journal.pone.0031220
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A Novel Framework for the Comparative Analysis of Biological Networks

Abstract: Genome sequencing projects provide nearly complete lists of the individual components present in an organism, but reveal little about how they work together. Follow-up initiatives have deciphered thousands of dynamic and context-dependent interrelationships between gene products that need to be analyzed with novel bioinformatics approaches able to capture their complex emerging properties. Here, we present a novel framework for the alignment and comparative analysis of biological networks of arbitrary topology… Show more

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Cited by 44 publications
(86 citation statements)
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“…We tested NetAligner under different configurations and input data, including the original proteomes and homologies provided with the tool. According to our analysis NetAligner achieves the best performance when using the predict likely conserved interactions setting, together with the parameters suggested in its reference paper [16]. NetAligner extracts a bigger and more reliable set of alignments on its own dataset.…”
Section: Resultsmentioning
confidence: 89%
“…We tested NetAligner under different configurations and input data, including the original proteomes and homologies provided with the tool. According to our analysis NetAligner achieves the best performance when using the predict likely conserved interactions setting, together with the parameters suggested in its reference paper [16]. NetAligner extracts a bigger and more reliable set of alignments on its own dataset.…”
Section: Resultsmentioning
confidence: 89%
“…Conserved Subnetworks-To identify conserved subnetworks in the H. pylori PIM compared with other bacterial interactomes we used Netaligner (59,60) and extracted alignments with p Ͻ 0.01. We then looked for enriched GO terms to identify the role of complexes.…”
Section: Cloning Yeast Two-hybrid Screens and Pairwise Testscloningmentioning
confidence: 99%
“…However, cancer is a complex disease arising from alterations in multiple pathways (biological/protein networks) [2] that have evolved to be very robust [3] and designing drugs against single proteins has yet to yield optimal clinical success [4]. As they are fundamental organizing principles of life, the removal of individual components through single protein-targeted drugs from such networks has surprisingly little functional consequence, even in pathological states of cancer.…”
mentioning
confidence: 99%