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dbWGFP: a database and web server of human whole-genome single nucleotide variants and their functional predictions
The recent advancement of the next generation sequencing technology has enabled the fast and low-cost detection of all genetic variants spreading across the entire human genome, making the application of whole-genome sequencing a tendency in the study of disease-causing genetic variants. Nevertheles...
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| Pubblicato in: | Database (Oxford) |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4795934/ https://ncbi.nlm.nih.gov/pubmed/26989155 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/database/baw024 |
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