Mapping and characterization of structural variation in 17,795 human genomes

A key goal of whole genome sequencing (WGS) for human genetics studies is to interrogate all forms of variation, including single nucleotide variants (SNV), small insertion/deletion (indel) variants and structural variants (SV). However, tools and resources for the study of SV have lagged behind tho...

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Detalles Bibliográficos
Autores principales: Abel, Haley J., Larson, David E., Regier, Allison A., Chiang, Colby, Das, Indraniel, Kanchi, Krishna L., Layer, Ryan M., Neale, Benjamin M., Salerno, William J., Reeves, Catherine, Buyske, Steven, Matise, Tara C., Muzny, Donna M., Zody, Michael C., Lander, Eric S., Dutcher, Susan K., Stitziel, Nathan O., Hall, Ira M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547914/
https://www.ncbi.nlm.nih.gov/pubmed/32460305
http://dx.doi.org/10.1038/s41586-020-2371-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547914/
https://www.ncbi.nlm.nih.gov/pubmed/32460305
http://dx.doi.org/10.1038/s41586-020-2371-0

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