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VCF‐Server: A web‐based visualization tool for high‐throughput variant data mining and management
BACKGROUND: Next‐generation sequencing (NGS) has been widely used in both clinics and research. It has become the most powerful tool for diagnosing genetic disorders and investigating disease etiology through the discovery of genetic variants. Variants identified by NGS are stored in variant call fo...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625089/ https://www.ncbi.nlm.nih.gov/pubmed/31127704 http://dx.doi.org/10.1002/mgg3.641 |