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Interpreting the impact of noncoding structural variation in neurodevelopmental disorders

The emergence of novel sequencing technologies has greatly improved the identification of structural variation, revealing that a human genome harbors tens of thousands of structural variants (SVs). Since these SVs primarily impact noncoding DNA sequences, the next challenge is one of interpretation,...

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Detalles Bibliográficos
Autores principales: D’haene, Eva, Vergult, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7790743/
https://www.ncbi.nlm.nih.gov/pubmed/32973355
http://dx.doi.org/10.1038/s41436-020-00974-1

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