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Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease
Copy number variants (CNVs) are significant contributors to the pathogenicity of rare genetic diseases and with new innovative methods can now reliably be identified from exome sequencing. Challenges still remain in accurate classification of CNV pathogenicity. CNV calling using GATK-gCNV was perfor...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593084/ https://www.ncbi.nlm.nih.gov/pubmed/37873196 http://dx.doi.org/10.1101/2023.10.05.23296595 |