Detalles del proyecto
Description
Project Narrative:
The functional interpretation of genetic variation in diseases faces critical roadblocks, due to the lack of
scalable methods to assess the significance of candidate variants experimentally, while accounting for
genomic context. This proposal introduces a morphological profiling method, that is able to rapidly identify
disease-associated phenotypes in patient cells and offers a cost-efficient and unbiased way to determine the
significance of putative pathogenic variants at scale. If successful, this proposal will establish cellular profiling
of patient cells as a powerful platform to advance genomic and translational medicine.
Estado | Finalizado |
---|---|
Fecha de inicio/Fecha fin | 12/22/20 → 11/30/22 |
Financiación
- National Human Genome Research Institute: $97,780.00
- National Human Genome Research Institute: $97,904.00
Keywords
- Genética
- Inteligencia artificial
- Genética (clínica)
Huella digital
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