Opendata, web and dolomites

DeepRNA SIGNED

Discovering functional protein-RNA interactions through data integration and machine learning.

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 DeepRNA project word cloud

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

disease    track    aggregation    determined    medicine    enabled    spinocerebellar    splicing    interactome    amyotrophic    tools    thereby    group    loci    aiding    complementing    disorders    graph    standard    polymorphisms    threatening    diamond    trait    host    domain    interdisciplinary    computing    molecular    translation    sclerosis    personalised    ranging    maintaining    protein    expand    genomic    recognised    diseases    heterogeneous    als    creatively    life    associations    am    experimentally    genome    validating    rna    ataxia    team    encoding    quantitative    interaction    record    confident    independence    implicated    network    skills    predictions    signalling    dataset    rationalise    expression    variants    352    mechanisms    quality    medically    anaemia    deeprna    blackfan    neural    data    fellowship    human    defects    experimental    examples    542    manner    globally    employ    spectrum    rnas    eqtl    transferrable    partitioning    interactions    gold    equip    proteins    me    accuracy    transcriptome    binding    confidently    eqtls    lateral    genetic    complemented   

Project "DeepRNA" data sheet

The following table provides information about the project.

Coordinator
FUNDACIO CENTRE DE REGULACIO GENOMICA 

Organization address
address: CARRER DOCTOR AIGUADER 88
city: BARCELONA
postcode: 8003
website: www.crg.es

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 Spain [ES]
 Total cost 158˙121 €
 EC max contribution 158˙121 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-03-01   to  2020-02-29

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACIO CENTRE DE REGULACIO GENOMICA ES (BARCELONA) coordinator 158˙121.00

Map

 Project objective

RNA-binding proteins are implicated across a wide spectrum of human genetic disorders, with molecular mechanisms ranging from aggregation of proteins and RNAs to defects in splicing and translation. Examples include heterogeneous and life-threatening genetic disorders such as Diamond-Blackfan anaemia, spinocerebellar ataxia and amyotrophic lateral sclerosis (ALS) among others.

The DeepRNA project targets genetic diseases via disease-associated variants in the human transcriptome and is enabled by recent data on expression quantitative trait loci (eQTLs) and experimentally determined RNA-protein and RNA-RNA interactions. The data will be complemented with high-quality RNA-protein interaction predictions carried out in the host group that has a strong track record in computing and validating RNA-protein associations.

To my knowledge the use of eQTL variants to study RNA-protein interactions is a novel approach and is useful for developing new tools for personalised medicine. My approach will expand the human interactome in a genome-wide manner beyond experimental data, which is currently available for only 352 of the 1,542 recently described RNA-binding proteins. Complementing experimentally determined interactions with predictions will allow me to expand my analyses of the human interactome to the genomic scale while maintaining accuracy, by using the experimental dataset as a gold standard. I will employ methods such as graph partitioning and graph neural network encoding to rationalise the effects of disease-associated variants on the human interaction network, and make quantitative predictions of polymorphisms associated with genetic diseases, thereby aiding personalised medicine.

I am confident that this fellowship will equip me with the domain knowledge, independence and transferrable skills to confidently and creatively build an interdisciplinary, globally recognised research team within Europe that will focus on medically relevant human signalling systems.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "DEEPRNA" 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 "DEEPRNA" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

NSTree (2020)

Understanding substrate delivery for cell wall biosynthesis in plants

Read More  

CREDit (2020)

Chronological REference Datasets and Sites (CREDit) towards improved accuracy and precision in luminescence-based chronologies

Read More  

MemoryAggregates (2020)

Mechanism of Whi3 Aggregation and its Age-dependent Malfunction

Read More