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A novel copy number variants kernel association test with application to autism spectrum disorders studies
Motivation: Copy number variants (CNVs) have been implicated in a variety of neurodevelopmental disorders, including autism spectrum disorders, intellectual disability and schizophrenia. Recent advances in high-throughput genomic technologies have enabled rapid discovery of many genetic variants inc...
Gardado en:
| Publicado en: | Bioinformatics |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5181531/ https://ncbi.nlm.nih.gov/pubmed/27497442 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw500 |
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