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MultiDCoX: Multi-factor analysis of differential co-expression.
Liany, Herty; Rajapakse, Jagath C; Karuturi, R Krishna Murthy.
Afiliación
  • Liany H; School of Computing, National University of Singapore, 21 Lower Kent Ridge Rd, Singapore, 119077, Singapore.
  • Rajapakse JC; Computational and System Biology, Genome Institute of Singapore, A-STAR, 60 Biopolis Street, Singapore, 138672, Singapore.
  • Karuturi RKM; School of Computer Science and Engineering, Nanyang Technological University, 50 Nanyang Ave, Singapore, 639798, Singapore.
BMC Bioinformatics ; 18(Suppl 16): 576, 2017 12 28.
Article en En | MEDLINE | ID: mdl-29297310
ABSTRACT

BACKGROUND:

Differential co-expression (DCX) signifies change in degree of co-expression of a set of genes among different biological conditions. It has been used to identify differential co-expression networks or interactomes. Many algorithms have been developed for single-factor differential co-expression analysis and applied in a variety of studies. However, in many studies, the samples are characterized by multiple factors such as genetic markers, clinical variables and treatments. No algorithm or methodology is available for multi-factor analysis of differential co-expression.

RESULTS:

We developed a novel formulation and a computationally efficient greedy search algorithm called MultiDCoX to perform multi-factor differential co-expression analysis. Simulated data analysis demonstrates that the algorithm can effectively elicit differentially co-expressed (DCX) gene sets and quantify the influence of each factor on co-expression. MultiDCoX analysis of a breast cancer dataset identified interesting biologically meaningful differentially co-expressed (DCX) gene sets along with genetic and clinical factors that influenced the respective differential co-expression.

CONCLUSIONS:

MultiDCoX is a space and time efficient procedure to identify differentially co-expressed gene sets and successfully identify influence of individual factors on differential co-expression.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Algoritmos / Regulación de la Expresión Génica / Análisis Factorial / Redes Reguladoras de Genes Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: BMC Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Singapur

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Algoritmos / Regulación de la Expresión Génica / Análisis Factorial / Redes Reguladoras de Genes Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: BMC Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Singapur