RNAREGMAP

Condition specific RNA Regulatory Maps

 Coordinatore MAX-DELBRUCK-CENTRUM FUR MOLEKULARE MEDIZIN IN DER HELMHOLTZ-GEMEINSCHAFT 

 Organization address address: ROBERT ROSSLE STRASSE 10
city: BERLIN
postcode: 13125

contact info
Titolo: Dr.
Nome: Ioannis
Cognome: Legouras
Email: send email
Telefono: 493094000000

 Nazionalità Coordinatore Germany [DE]
 Totale costo 168˙794 €
 EC contributo 168˙794 €
 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-2012-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-06-01   -   2015-05-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    MAX-DELBRUCK-CENTRUM FUR MOLEKULARE MEDIZIN IN DER HELMHOLTZ-GEMEINSCHAFT

 Organization address address: ROBERT ROSSLE STRASSE 10
city: BERLIN
postcode: 13125

contact info
Titolo: Dr.
Nome: Ioannis
Cognome: Legouras
Email: send email
Telefono: 493094000000

DE (BERLIN) coordinator 168˙794.40

Mappa


 Word cloud

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computational    mrna    experimental    interactions    rbps    protein    regulatory    binding    adrenal    occupancy    rna    combined    profiles    rbp    modeling   

 Obiettivo del progetto (Objective)

'RNA-binding proteins (RBPs) regulate the processing and expression of protein-coding transcripts. The goal of the proposed research is to develop a strategy to determine specific mRNA regulatory factors and elements important for investigating any biological processes. First, we will construct a transcriptome-wide post-transcriptional regulatory map of RBP-mRNA interactions by probabilistic modeling of protein occupancy profiles and RNA sequence data, simultaneously inferring binding locations of numerous of RBPs for a specific experimental condition. Next, we will predict specific RBPs with important regulatory functions in a different experimental setting by applying our model to protein occupancy profiles generated from different cellular conditions. Specifically, we will generate protein occupancy profiles for a human adrenocortical cell line stimulated with the primary physiological regulators of adrenal steroid hormones to examine the production of mineralocorticoids, glucocorticoids, and adrenal androgens. This research proposal necessitates a combined wet/dry approach including the complete cycle of genome-wide predictive modeling and experimental validations. The research in this proposal benefits from the molecular biology and genomics background of the Experienced Researcher combined with the computational modeling expertise of the Host Laboratory. This research has transformative potential for the field by effectively learning specific RBP-mRNA interactions from computational modeling of a single experiment.'

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