dbVar structural variant cluster set for data analysis and variant comparison

dbVar houses over 3 million submitted structural variants (SSV) from 120 human studies including copy number variations (CNV), insertions, deletions, inversions, translocations, and complex chromosomal rearrangements. Users can submit multiple SSVs to dbVAR  that are presumably identical, but were a...

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Detalles Bibliográficos
Autores principales: Phan, Lon, Hsu, Jeffrey, Tri, Le Quang Minh, Willi, Michaela, Mansour, Tamer, Kai, Yan, Garner, John, Lopez, John, Busby, Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Software Tool Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345777/
https://www.ncbi.nlm.nih.gov/pubmed/28357035
http://dx.doi.org/10.12688/f1000research.8290.2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345777/
https://www.ncbi.nlm.nih.gov/pubmed/28357035
http://dx.doi.org/10.12688/f1000research.8290.2

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