CNVDeep: deep association of copy number variants with neurocognitive disorders
Abstract Background Copy number variants (CNVs) have become increasingly instrumental in understanding the etiology of all diseases and phenotypes, including Neurocognitive Disorders (NDs). Among the well-established regions associated with ND are small parts of chromosome 16 deletions (16p11.2) and...
Sábháilte in:
| Príomhchruthaitheoirí: | , , |
|---|---|
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
BMC
2024-08-01
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| Sraith: | BMC Bioinformatics |
| Ábhair: | |
| Rochtain ar líne: | https://doi.org/10.1186/s12859-024-05874-8 |
| Clibeanna: |
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