Human Genetic

ALPS WGS + RNA-Seq

Comprehensive genomicand transcriptional characterization of the Autoimmune Lymphoproliferative Syndrome (ALPS): Whole Genome Sequencing and RNA-seq profiling of a representative panel offamilies withclinical incomplete penetrance

Antonio Rausell
Imagine Institute Paris

CIMP-DRIVE

Discovery of noncoding genetic drivers implicated in the aggressive CpG-island methylator phenotype(CIMP)in adrenocortical carcinom

Valentina Boeva
Institute Cochin-INSERM-Université Paris Descartes Paris

MARIO

Genomic characterisation of metastatic breast cancers

Fabrice Andre
INSERM-Gustave Roussy Villejuif

K-Rare

Contribution of rare variants to kidney cancer genetic susceptibility Génétique Humaine

Estelle Chanudet
INSERM U1162 Paris

HetHCC

Deciphering the heterogeneous genome-microenvironment interplay in hepatocellular carcinomas

Jessica Zucman-Rossi
INSERM U1162 Paris

ALLOGENOMICS

Whole exome sequencing inlivingDonor/Recipient kidney transplants

Laurent Mesnard
INSERM-IMR 1155-Hôpital Tenon Paris

FCD-Genomics

Large scale genomic, expression and epigenetic studies to better understand Genetic, molecular and cellular pathology of focal cortical dysplasia (FCD)

Jamel Chelly
IGBMC Strasbourg

GENTAUMIX

GENomic and Transcriptomic Analysis of Undiagnosed Myalgia Induced by eXercise

Fabrice Rannou
Physiology Department- CHRU Cavale Blanche Brest

Mitral Valve-Seq

A sequencing-based genome-wide association study on Mitral Valve Disease

Jean-Jacques Schott
Inserm-Institut du Thorax Nantes

CAT-SEQ

Molecular characterization offelinelow grade alimentary lymphoma, a spontaneous animal model of human indolent T-cell lymphoproliferative disorder of the gastrointestinal tract

Lucile Couronné
Unité INSERM-Intitut Imagine Paris