OVAS: an open-source variant analysis suite with inheritance modelling

BACKGROUND: The advent of modern high-throughput genetics continually broadens the gap between the rising volume of sequencing data, and the tools required to process them. The need to pinpoint a small subset of functionally important variants has now shifted towards identifying the critical differe...

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Detalles Bibliográficos
Autores principales: Mozere, Monika, Tekman, Mehmet, Kari, Jameela, Bockenhauer, Detlef, Kleta, Robert, Stanescu, Horia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806474/
https://www.ncbi.nlm.nih.gov/pubmed/29422027
http://dx.doi.org/10.1186/s12859-018-2030-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806474/
https://www.ncbi.nlm.nih.gov/pubmed/29422027
http://dx.doi.org/10.1186/s12859-018-2030-8

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