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Genetics Core

$288,513P30FY2025AGNIH

Columbia University Health Sciences, New York NY

Investigators

Linked publications, trials & patents

Abstract

GENETICS CORE SUMMARY This new application will build on our work of the three previous funding cycles in which we established the Human Genetics Core (HGC) as an essential part of the Columbia ADRC. The HGC provides a centralized resource for the organization and analysis of genetic data within the ADRC and projects affiliated with the ADRC at Columbia University by providing the full physical and intellectual infrastructure needed to coordinate genetic research efforts and provide a platform for investigators to create a better understanding of genotype-phenotype relationships for dementia and related endophenotypes. Specifically, the HGC will: (1) provide a genetic material repository to process, extract, store and distribute genetic material from patients and controls, and track the collection and usage of genetic material; (2) provide a genetic database for storage, handling, preparation and distribution of genomic data from ADRC subjects and large-scale datasets available to the ADRC; (3) provide a high-end cluster environment and analytical support in statistical genetics and bioinformatics to facilitate genomic data analysis; and (4) extend the largescale genomic data available on this ADRC sample (ie. GWAS, WGS/WES, eQTL maps), and comprehensively characterize subjects for genetic variation in the amyloid, tau, immune response, and endosomal trafficking pathways as well as genetic ancestry. In line with our vision for precision medicine, this characterization will move us forward to i) provide investigators with a backbone for more targeted research informed by genetic background, ii) disentangle potential pathophysiologic heterogeneity in this cohort, and iii) explore a variety of critical questions addressing the Thematic Aim by integration with the extensive translational data generated by the Neuropathology, Biomarker and Neuroimmunology Cores.

View original record on NIH RePORTER →