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Abstract
Alinejad-Rokny et al. develop a tool, SNATCNV, to analyze CNV associations in genetic diseases and disorders. By application of SNATCNV to an autism cohort, they generate a high-confidence map of autism-associated CNVs and provide full lists of brain-enriched coding and lncRNA genes.
Original language | English |
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Article number | 108307 |
Journal | Cell Reports |
Volume | 33 |
Issue number | 4 |
DOIs | |
Publication status | Published - 27 Oct 2020 |
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Dive into the research topics of 'Brain-Enriched Coding and Long Non-coding RNA Genes Are Overrepresented in Recurrent Neurodevelopmental Disorder CNVs'. Together they form a unique fingerprint.Projects
- 1 Finished
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Systems Biology of Human Disease
Forrest, A. (Investigator 01)
NHMRC National Health and Medical Research Council
1/01/19 → 31/12/23
Project: Research