Cargando…

f-divergence cutoff index to simultaneously identify differential expression in the integrated transcriptome and proteome

The ability to integrate ‘omics’ (i.e. transcriptomics and proteomics) is becoming increasingly important to the understanding of regulatory mechanisms. There are currently no tools available to identify differentially expressed genes (DEGs) across different ‘omics’ data types or multi-dimensional d...

Descripción completa

Detalles Bibliográficos
Autores principales: Tang, Shaojun, Hemberg, Martin, Cansizoglu, Ertugrul, Belin, Stephane, Kosik, Kenneth, Kreiman, Gabriel, Steen, Hanno, Steen, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889934/
https://www.ncbi.nlm.nih.gov/pubmed/26980280
http://dx.doi.org/10.1093/nar/gkw157
Descripción
Sumario:The ability to integrate ‘omics’ (i.e. transcriptomics and proteomics) is becoming increasingly important to the understanding of regulatory mechanisms. There are currently no tools available to identify differentially expressed genes (DEGs) across different ‘omics’ data types or multi-dimensional data including time courses. We present fCI (f-divergence Cut-out Index), a model capable of simultaneously identifying DEGs from continuous and discrete transcriptomic, proteomic and integrated proteogenomic data. We show that fCI can be used across multiple diverse sets of data and can unambiguously find genes that show functional modulation, developmental changes or misregulation. Applying fCI to several proteogenomics datasets, we identified a number of important genes that showed distinctive regulation patterns. The package fCI is available at R Bioconductor and http://software.steenlab.org/fCI/.