GenESysV: a fast, intuitive and scalable genome exploration open source tool for variants generated from high-throughput sequencing projects

BACKGROUND: High throughput sequencing technologies have been increasingly used in basic genetic research as well as in clinical applications. More and more variants underlying Mendelian and complex diseases are being discovered and documented using these technologies. However, identifying and obtai...

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Detalles Bibliográficos
Autores principales: Zia, Mohammad, Spurgeon, Paul, Levesque, Adrian, Furlani, Thomas, Wang, Jianxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357466/
https://www.ncbi.nlm.nih.gov/pubmed/30704396
http://dx.doi.org/10.1186/s12859-019-2636-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357466/
https://www.ncbi.nlm.nih.gov/pubmed/30704396
http://dx.doi.org/10.1186/s12859-019-2636-5

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