Détails sur le projet
Description
PROJECT NARRATIVE
The clinical utility of whole genome sequencing to diagnose rare inherited conditions is significantly limited by
our inability to interpret variants in the non-coding regions of the genome. This is particularly relevant since
misregulation of a relatively new class of non-coding genes, dubbed long non-coding RNAs (lncRNAs), has been
implicated in numerous inherited conditions, including neurodevelopmental disorders, but how these genes are
normally regulated is understudied. This proposal takes a two-pronged approach to address these limitations
through studying the spatiotemporal regulation of a lncRNA that is required for proper neuronal maturation, and
by applying statistical genetics-based approaches to curate putative pathogenic non-coding variants in patients
with neurodevelopmental disorders.
Statut | Terminé |
---|---|
Date de début/de fin réelle | 1/20/21 → 11/30/22 |
Financement
- National Institute of Neurological Disorders and Stroke: 193 536,00 $ US
- National Institute of Neurological Disorders and Stroke: 193 536,00 $ US
Keywords
- Genética
- Biología molecular
Empreinte numérique
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