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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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| Publicado no: | F1000Res |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
F1000Research
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5345777/ https://ncbi.nlm.nih.gov/pubmed/28357035 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.8290.2 |
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