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.

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

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.)

AST (2019)

Automatic System Testing

Read More  

CHIPTRANSFORM (2018)

On-chip optical communication with transformation optics

Read More  

HEIST (2020)

High-temperature Electrochemical Impedance Spectroscopy Transmission electron microscopy on energy materials

Read More