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SMCKAT, a Sequential Multi-Dimensional CNV Kernel-Based Association Test
Copy number variants (CNVs) are the most common form of structural genetic variation, reflecting the gain or loss of DNA segments compared with a reference genome. Studies have identified CNV association with different diseases. However, the association between the sequential order of CNVs and disea...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709152/ https://www.ncbi.nlm.nih.gov/pubmed/34947833 http://dx.doi.org/10.3390/life11121302 |