RAUMN

Reconstruction and understanding of molecular networks

 Coordinatore BAR ILAN UNIVERSITY 

 Organization address address: BAR ILAN UNIVERSITY CAMPUS
city: RAMAT GAN
postcode: 52900

contact info
Titolo: Ms.
Nome: Estelle
Cognome: Waise
Email: send email
Telefono: 97235317439
Fax: 97236353277

 Nazionalità Coordinatore Israel [IL]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2009-RG
 Funding Scheme MC-IRG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-04-01   -   2014-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    BAR ILAN UNIVERSITY

 Organization address address: BAR ILAN UNIVERSITY CAMPUS
city: RAMAT GAN
postcode: 52900

contact info
Titolo: Ms.
Nome: Estelle
Cognome: Waise
Email: send email
Telefono: 97235317439
Fax: 97236353277

IL (RAMAT GAN) coordinator 100˙000.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

biology    molecules    functional    signaling    cellular    patterns    network    reconstruct    pathways    percent    molecular    data    interact    pathway    metabolic   

 Obiettivo del progetto (Objective)

'A major challenge for current biology is to understand how bio-molecules interact and cooperate to achieve their joint cellular functions. Understanding a pathway requires that we first reconstruct the network - identify what molecules participate in a given pathway and how they interact, and then characterize its functional modes. Following the explosion of genome wide assays, network reconstruction became a central task in molecular biology, spanning signaling, metabolic, and regulatory pathways. However, despite intensive research, many fundamental cellular pathways are only partially known, and not well understood. For instance, in the metabolic pathways of S. cerevisiae, perhaps the best understood biochemical network, 20 percent of enzymes and transporters are unidentified. In the same organism, only 30 percent of the interactions in the signaling pathways are known. The goal of the research proposed here is to develop computational and statistical methods for completing partially known biological pathways and use these methods to reconstruct and understand two important molecular pathways: metabolic pathways and signal transduction pathways. This will be achieved by learning how diverse functional data maps onto known networks, identifying recurring patterns of this mapping, and use them to predict unknown network components. We have recently showed how these patterns, which we call “activity motifs”, can be identified from data, and reveal organization principles of metabolic and signaling pathways1-2.'

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