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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,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group US
2020
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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 |