Discovery and genotyping of structural variation from long-read haploid genome sequence data

In an effort to more fully understand the full spectrum of human genetic variation, we generated deep single-molecule, real-time (SMRT) sequencing data from two haploid human genomes. By using an assembly-based approach (SMRT-SV), we systematically assessed each genome independently for structural v...

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Detalles Bibliográficos
Autores principales: Huddleston, John, Chaisson, Mark J.P., Steinberg, Karyn Meltz, Warren, Wes, Hoekzema, Kendra, Gordon, David, Graves-Lindsay, Tina A., Munson, Katherine M., Kronenberg, Zev N., Vives, Laura, Peluso, Paul, Boitano, Matthew, Chin, Chen-Shin, Korlach, Jonas, Wilson, Richard K., Eichler, Evan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411763/
https://www.ncbi.nlm.nih.gov/pubmed/27895111
http://dx.doi.org/10.1101/gr.214007.116

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411763/
https://www.ncbi.nlm.nih.gov/pubmed/27895111
http://dx.doi.org/10.1101/gr.214007.116

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