dbVar structural variant cluster set for data analysis and variant comparison [version 2; referees: 2 approved]
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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| Autores principales: | , , , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
F1000 Research Ltd
2017-02-01
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| Colección: | F1000Research |
| Materias: | |
| Acceso en línea: | https://f1000research.com/articles/5-673/v2 |
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