MinorityReport, software for generalized analysis of causal genetic variants

BACKGROUND: The widespread availability of next generation genome sequencing technologies has enabled a wide range of variant detection applications, especially in cancer and inborn genetic disorders. For model systems and microorganisms, the same technology may be used to discover the causative mut...

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Detalles Bibliográficos
Autores principales: Horst, Jeremy A., Wu, Wesley, DeRisi, Joseph L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324306/
https://www.ncbi.nlm.nih.gov/pubmed/28231785
http://dx.doi.org/10.1186/s12936-017-1730-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324306/
https://www.ncbi.nlm.nih.gov/pubmed/28231785
http://dx.doi.org/10.1186/s12936-017-1730-2

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