Abstract
Protein–protein interactions play a major role in most cellular processes. Thus, the challenge
of identifying the full repertoire of interacting proteins in the cell is of great importance and
has been addressed both experimentally and computationally. Today, large scale experimental
studies of protein interactions, while partial and noisy, allow us to characterize properties
of interacting proteins and develop predictive algorithms. Most existing algorithms, however,
ignore possible dependencies between interacting pairs and predict them independently of
one another. In this study, we present a computational approach that overcomes this drawback
by predicting protein–protein interactions simultaneously. In addition, our approach
allows us to integrate various protein attributes and explicitly account for uncertainty of
assay measurements. Using the language of
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