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EpiNoise SIGNED

The role of epigenetic heterogeneity in cell fate decisions

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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Project "EpiNoise" data sheet

The following table provides information about the project.

Coordinator
THE BABRAHAM INSTITUTE 

Organization address
address: Babraham Hall
city: CAMBRIDGE
postcode: CB22 3AT
website: www.babraham.ac.uk

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 United Kingdom [UK]
 Total cost 183˙454 €
 EC max contribution 183˙454 € (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 2019
 Duration (year-month-day) from 2019-09-01   to  2021-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE BABRAHAM INSTITUTE UK (CAMBRIDGE) coordinator 183˙454.00

Map

 Project objective

A fundamental question in biology is how different cell fates are generated. While it is clear that extensive remodelling of chromatin accessibility and DNA methylation is an essential step in early mammalian development, their roles in cell fate specification remain unclear. Furthermore, it is not known to what extent cell-to-cell differences in gene expression regulation affect cell fate decisions. The aim of this proposal is to uncover the roles of chromatin accessibility and DNAme in gene regulation and in cell fate specification during mouse development. I will use a novel sequencing approach for combined profiling of chromatin accessibility, DNA methylation and transcription in single cells as well as other state-of-the-art technologies to provide unique insights in the connection between chromatin accessibility, DNAme and transcription at the single cell level. Moreover, this proposal has the potential to drastically change our view of germ layer specification by highlighting the role of cellular heterogeneity in this process. Together, this will improve our understanding of both pluripotency and differentiation, advancing the fields of stem cell research and development. The proposed research combines my experience in the areas of cellular heterogeneity and multidisciplinary science with the host’s experience in single cell genomics, epigenetics and mouse development. The knowledge and skills gained from this project combined with my scientific and personal development will prepare me for my goal of establishing my own academic research group.

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

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