Grant: Operating Grant
Université du Québec à Chicoutimi
$1,021,307.00
Genomic risk in asthma susceptibility accessed by next-generation integrative tools
FY 2013-14
Summary
Asthma is a chronic respiratory disease, which afflicts patients of all ages, causes important morbidity and mortality and, consequently, generates substantial costs to our society. Although its pathogenesis remains largely undefined, we know that genetic and environmental factors play an important role. In this study, we intend to benefits of two large asthma familial studies from populations that have a common genetic background (French Canadian and French) to integrate the genetics and epigenetics data in aims to increase our knowledge of the impact of genetics and environment in the natural history of asthma. Precisely, we aim to identify rare variants and characterize the epigenetic profiling to integrate the changes in relationship with asthma and allergic condition. With our unique familial asthma collections, new genomic data and novel genomic tools, we are in prime position to extend asthma genomics to unexplored areas. Our preliminary results provide strong indication that new risk factors will be discovered yielding insight to pathogenesis of asthma and offering an original approach to investigate the genetic of frequent disorders.
Department
Program
Operating Grant
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
293114
Name
Laprise Catherine
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Not applicable / Specified
Prcname2
Genetics
Projecttitle
Genomic risk in asthma susceptibility accessed by next-generation integrative tools
Programtype2
Operating Grants
Orgnameinp2
Université du Québec à Chicoutimi
Cihramount2
$1,021,307
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Asthma; Atopy; Epigenomics; Genetic Associations; Methylome; Rare Variant; Regulome; Sequencing
Abstract
Asthma is a chronic respiratory disease, which afflicts patients of all ages, causes important morbidity and mortality and, consequently, generates substantial costs to our society. Although its pathogenesis remains largely undefined, we know that genetic and environmental factors play an important role. In this study, we intend to benefits of two large asthma familial studies from populations that have a common genetic background (French Canadian and French) to integrate the genetics and epigenetics data in aims to increase our knowledge of the impact of genetics and environment in the natural history of asthma. Precisely, we aim to identify rare variants and characterize the epigenetic profiling to integrate the changes in relationship with asthma and allergic condition. With our unique familial asthma collections, new genomic data and novel genomic tools, we are in prime position to extend asthma genomics to unexplored areas. Our preliminary results provide strong indication that new risk factors will be discovered yielding insight to pathogenesis of asthma and offering an original approach to investigate the genetic of frequent disorders.
Competitiondate
201309
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Laprise, Catherine; Pastinen, Tomi
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,021,307~ $0~