GAGE: generally applicable gene set enrichment for pathway analysis
By Weijun Luo, M. Friedman, Kerby Shedden, K. Hankenson, P. Woolf. BMC Bioinformatics, 2009
1,085 citations recorded by the source corpus.
BackgroundGene set analysis (GSA) is a widely used strategy for gene expression data analysis based on pathway knowledge. GSA focuses on sets of related genes and has established major advantages over individual gene analyses, including greater robustness, sensitivity and biological relevance. However, previous GSA methods have limited usage as they cannot handle datasets of different sample sizes or experimental designs.ResultsTo address these limitations, we present a new GSA method called Generally Applicable Gene-set Enrichment (GAGE). We successfully apply GAGE to multiple microarray datasets with different sample sizes, experimental designs and profiling techniques. GAGE shows significantly better results when compared to two other commonly used GSA methods of GSEA and PAGE. We demonstrate this improvement in the following three aspects: (1) consistency across repeated studies/experiments; (2) sensitivity and specificity; (3) biological relevance of the regulatory mechanisms inferred.GAGE reveals novel and relevant regulatory mechanisms from both published and previously unpublished microarray studies. From two published lung cancer data sets, GAGE derived a more cohesive and predictive mechanistic scheme underlying lung cancer progress and metastasis. For a previously unpublished BMP6 study, GAGE predicted novel regulatory mechanisms for BMP6 induced osteoblast differentiation, including the canonical BMP-TGF beta signaling, JAK-STAT signaling, Wnt signaling, and estrogen signaling pathways–all of which are supported by the experimental literature.ConclusionGAGE is generally applicable to gene expression datasets with different sample sizes and experimental designs. GAGE consistently outperformed two most frequently used GSA methods and inferred statistically and biologically more relevant regulatory pathways. The GAGE method is implemented in R in the "gage" package, available under the GNU GPL from http://sysbio.engin.umich.edu/~luow/downloads.php.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/675da7ce40878870e42846d66b3dbbdf67f6f9a2
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In Molecular Biology
- Michael Pollak
- J. St-Pierre
- Lei Kong
- Yi Zhao
- Eyal Gottlieb
- Nahum Sonenberg
- Weijun Luo
- Cory R. Brouwer
Citations in the corpus
- High-level adherence to a Mediterranean diet beneficially impacts the gut microbiota and associated metabolome (2015, neutral): “45”
- Pathview Web: user friendly pathway visualization and data integration (2017, positive): “The In the pathway analysis step, generally applicable gene-set enrichment (GAGE) is used for numeric data and over representation analysis for categorical data.”
- KOBAS-i: intelligent prioritization and exploratory visualization of biological functions for gene enrichment analysis (2021, positive): “It integrates seven widely used FCS methods: GSEA (14), GSA (16), PADOG (17), PLAGE (18), GAGE (19), GLOBALTEST (20) and SAFE (21) and two prominent PT methods: GANPA (23), and CEPA (24), into a single ensemble score (R score).”
- mTORC1 controls mitochondrial activity and biogenesis through 4E-BP-dependent translational regulation. (2013, positive): “We applied the ‘‘rank.test’’ option in GAGE using signed (direction of regulation) log10(FDR) as input data within the ‘‘gage’’ bioconductor package (Gentleman et al., 2004).”
- Camera: a competitive gene set test accounting for inter-gene correlation (2012, neutral): “Previous parametric gene set tests have been based on genewise logFCs, which typically have different variances for different genes (13,16).”