Opendata, web and dolomites

EnDeCAD SIGNED

Enhancers Decoding the Mechanisms Underlying CAD Risk

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 EnDeCAD project word cloud

Explore the words cloud of the EnDeCAD project. It provides you a very rough idea of what is the project "EnDeCAD" about.

noncoding    polymorphisms    gene    wall    phenotypic    molecular    macrophages    enhancers    smooth    regulatory    lying    vessel    coronary    discovered    portion    treatment    association    parallel    candidate    search    establishment    date    loci    additionally    link    artery    genetic    regions    causal    basis    expression    array    translatable    cardiovascular    clinical    massively    hope    ultimately    characterization    complete    deep    endothelial    breakthrough    small    eqtl    events    prediction    biological    cells    vast    discoveries    progression    linked    identification    mechanisms    hepatocytes    obtain    relationships    data    roles    gwas    single    hundreds    correlative    nucleotide    cell    majority    linking    genome    provides    interaction    driving    strives    cad    risk    trait    genes    understand    enhancer    types    biomarker    muscle    disease    snps    fundamental    adipocytes    function    metabolomics    pioneering    stimuli    explained    combination    significantly    heritability    functional    collection    variants    physical    picture    snp   

Project "EnDeCAD" data sheet

The following table provides information about the project.

Coordinator
ITA-SUOMEN YLIOPISTO 

Organization address
address: YLIOPISTONRANTA 1 E
city: KUOPIO
postcode: 70211
website: www.uef.fi

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Finland [FI]
 Total cost 1˙498˙647 €
 EC max contribution 1˙498˙647 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2023-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ITA-SUOMEN YLIOPISTO FI (KUOPIO) coordinator 1˙498˙647.00

Map

 Project objective

In recent years, genome-wide association studies (GWAS) have discovered hundreds of single nucleotide polymorphisms (SNPs) which are significantly associated with coronary artery disease (CAD). However, the SNPs identified by GWAS explain typically only small portion of the trait heritability and vast majority of variants do not have known biological roles. This is explained by variants lying within noncoding regions such as in cell type specific enhancers and additionally ‘the lead SNP’ identified in GWAS may not be the ‘the causal SNP’ but only linked with a trait associated SNP. Therefore, a major priority for understanding disease mechanisms is to understand at the molecular level the function of each CAD loci. In this study we aim to bring the functional characterization of SNPs associated with CAD risk to date by focusing our search for causal SNPs to enhancers of disease relevant cell types, namely endothelial cells, macrophages and smooth muscle cells of the vessel wall, hepatocytes and adipocytes. By combination of massively parallel enhancer activity measurements, collection of novel eQTL data throughout cell types under disease relevant stimuli, identification of the target genes in physical interaction with the candidate enhancers and establishment of correlative relationships between enhancer activity and gene expression we hope to identify causal enhancer variants and link them with target genes to obtain a more complete picture of the gene regulatory events driving disease progression and the genetic basis of CAD. Linking these findings with our deep phenotypic data for cardiovascular risk factors, gene expression and metabolomics has the potential to improve risk prediction, biomarker identification and treatment selection in clinical practice. Ultimately, this research strives for fundamental discoveries and breakthrough that advance our knowledge of CAD and provides pioneering steps towards taking the growing array of GWAS for translatable results.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "ENDECAD" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "ENDECAD" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

CohoSing (2019)

Cohomology and Singularities

Read More  

AST (2019)

Automatic System Testing

Read More  

RTMFRM (2019)

Room Temperature Magnetic Resonance Force Microscopy

Read More