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uGPA: unified Gene Pathway Analyzer package for high-throughput genome-wide screening data provides mechanistic overview on human diseases.
Ho, Daniel W H; Ng, Irene O L.
Afiliación
  • Ho DW; Department of Pathology, The University of Hong Kong, Hong Kong; State Key Laboratory for Liver Research, The University of Hong Kong, Hong Kong. Electronic address: dwhho@hku.hk.
  • Ng IO; Department of Pathology, The University of Hong Kong, Hong Kong; State Key Laboratory for Liver Research, The University of Hong Kong, Hong Kong.
Clin Chim Acta ; 441: 105-8, 2015 Feb 20.
Article en En | MEDLINE | ID: mdl-25549900
ABSTRACT

BACKGROUND:

Gene set or pathway analysis (GPA) can provide a comprehensive mechanistic overview in delineating molecular pathoetiology of human diseases. Existing tools that can handle for GPA on both mutational and gene expressional aspects are limited. This leads to the development of uGPA (unified Gene Pathway Analyzer).

METHODS:

uGPA package provides a unified solution to knowledge base-driven competitive GPA that can analyze genome-wide screening data derived from multiple platforms (next generation sequencing or microarray) and sample sources (genomic or transcriptomic) on both mutational and gene expressional perspectives. It allows for a quick assessment of perspective outline of gene sets on the studied disease through enrichment test modeled by cumulative hypergeometric distribution and reports the gene components detected with events (mutation or differential gene expression) in the gene sets.

RESULTS:

uGPA package has been successfully verified to be applicable on input data generated from NGS-based platforms (transcriptome sequencing and whole-exome sequencing). Genome-wide screening data from other platforms should also apply.

CONCLUSIONS:

uGPA package delivers a simple, flexible and platform-independent functionality to multiple aspects of GPA. It equips clinicians and scientists with a useful tool in studying molecular mechanism of human diseases using modern high-throughput genome-wide screening strategy, which assists personalized therapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Genoma Humano / Enfermedad / Secuenciación de Nucleótidos de Alto Rendimiento / Genes Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Clin Chim Acta Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Genoma Humano / Enfermedad / Secuenciación de Nucleótidos de Alto Rendimiento / Genes Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Clin Chim Acta Año: 2015 Tipo del documento: Article