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dc.contributor.authorTuncbag, Nurcan
dc.contributor.authorBraunstein, Alfredo
dc.contributor.authorPagnani, Andrea
dc.contributor.authorHuang, Shao-Shan Carol
dc.contributor.authorChayes, Jennifer
dc.contributor.authorBorgs, Christian
dc.contributor.authorZecchina, Riccardo
dc.contributor.authorFraenkel, Ernest
dc.contributor.authorTuncbag, Nurcan
dc.contributor.authorHuang, Shao-Shan Carol
dc.contributor.authorFraenkel, Ernest
dc.date.accessioned2013-07-09T20:25:00Z
dc.date.available2013-07-09T20:25:00Z
dc.date.issued2012-04
dc.identifier.isbn978-3-642-29626-0
dc.identifier.isbn978-3-642-29627-7
dc.identifier.isbn9783642296277
dc.identifier.issn0302-9743
dc.identifier.issn1611-3349
dc.identifier.urihttp://hdl.handle.net/1721.1/79429
dc.description.abstractSignaling networks are essential for cells to control processes such as growth and response to stimuli. Although many “omic” data sources are available to probe signaling pathways, these data are typically sparse and noisy. Thus, it has been difficult to use these data to discover the cause of the diseases. We overcome these problems and use “omic” data to simultaneously reconstruct multiple pathways that are altered in a particular condition by solving the prize-collecting Steiner forest problem. To evaluate this approach, we use the well-characterized yeast pheromone response. We then apply the method to human glioblastoma data, searching for a forest of trees each of which is rooted in a different cell surface receptor. This approach discovers both overlapping and independent signaling pathways that are enriched in functionally and clinically relevant proteins, which could provide the basis for new therapeutic strategies.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant U54CA112967)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant R01GM089903)en_US
dc.description.sponsorshipMassachusetts Institute of Technology (Eugene Bell Career Development Chair)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Award No. DB1- 082139)en_US
dc.description.sponsorshipEuropean Research Council (ERC grant OPTINF 267915)en_US
dc.description.sponsorshipEuropean Commission (EC grant STAMINA 265496)en_US
dc.language.isoen_US
dc.publisherSpringer Science + Business Media B.V.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/978-3-642-29627-7_31en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceProf. Fraenkel via Howard Silveren_US
dc.titleSimultaneous Reconstruction of Multiple Signaling Pathways via the Prize-Collecting Steiner Forest Problemen_US
dc.typeArticleen_US
dc.identifier.citationTuncbag, Nurcan, Alfredo Braunstein, Andrea Pagnani, Shao-Shan Carol Huang, Jennifer Chayes, Christian Borgs, Riccardo Zecchina, and Ernest Fraenkel. Simultaneous Reconstruction of Multiple Signaling Pathways via the Prize-Collecting Steiner Forest Problem. In Research in Computational Molecular Biology. Benny Chor, ed. Pp. 287–301. Berlin: Springer-Verlag Berlin Heidelberg, 2012. (Lecture notes in computer science; 7262).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.approverFraenkel, Ernsten_US
dc.contributor.mitauthorTuncbag, Nurcanen_US
dc.contributor.mitauthorHuang, Shao-Shan Carolen_US
dc.contributor.mitauthorFraenkel, Ernesten_US
dc.relation.journalProceedings of the International Conference on Research in Computational Molecular Biology, RECOMB 2012en_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/ConferencePaperen_US
eprint.statushttp://purl.org/eprint/status/NonPeerRevieweden_US
dspace.orderedauthorsTuncbag, Nurcan; Braunstein, Alfredo; Pagnani, Andrea; Huang, Shao-Shan Carol; Chayes, Jennifer; Borgs, Christian; Zecchina, Riccardo; Fraenkel, Ernesten_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9249-8181
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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