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GeMSTONE: orchestrated prioritization of human germline mutations in the cloud

Integrative analysis of whole-genome/exome-sequencing data has been challenging, especially for the non-programming research community, as it requires simultaneously managing a large number of computational tools. Even computational biologists find it unexpectedly difficult to reproduce results from...

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Detalles Bibliográficos
Autores principales: Chen, Siwei, Beltrán, Juan F., Esteban-Jurado, Clara, Franch-Expósito, Sebastià, Castellví-Bel, Sergi, Lipkin, Steven, Wei, Xiaomu, Yu, Haiyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556704/
https://www.ncbi.nlm.nih.gov/pubmed/28521008
http://dx.doi.org/10.1093/nar/gkx398
Descripción
Sumario:Integrative analysis of whole-genome/exome-sequencing data has been challenging, especially for the non-programming research community, as it requires simultaneously managing a large number of computational tools. Even computational biologists find it unexpectedly difficult to reproduce results from others or optimize their strategies in an end-to-end workflow. We introduce Germline Mutation Scoring Tool fOr Next-generation sEquencing data (GeMSTONE), a cloud-based variant prioritization tool with high-level customization and a comprehensive collection of bioinformatics tools and data libraries (http://gemstone.yulab.org/). GeMSTONE generates and readily accepts a shareable ‘recipe’ file for each run to either replicate previous results or analyze new data with identical parameters and provides a centralized workflow for prioritizing germline mutations in human disease within a streamlined workflow rather than a pool of program executions.