Project Details
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.
Status | Finished |
---|---|
Effective start/end date | 1/20/21 → 11/30/22 |
Funding
- National Institute of Neurological Disorders and Stroke: US$193,536.00
- National Institute of Neurological Disorders and Stroke: US$193,536.00
ASJC Scopus Subject Areas
- Genetics
- Molecular Biology
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