The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
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performing all the steps of gene expression meta-analysis considering the possible existence of missing genes. It provides the necessary functions to be able to perform the different methods of gene expression meta-analysis. In addition, it contains functions to apply quality controls, download GEO datasets and show graphical representations of the results.
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Perform a complete gene expression meta-analysis workflow including data preparation, annotation harmonization, log transformation, heterogeneity testing, optional imputation, meta-analysis, and heatmap visualization.
library(DExMA)
# Create meta-analysis object
phenoGroups <- c("condition", "condition", "state", "state")
phenoCases <- list(Study1 = "Diseased", Study2 = c("Diseased", "ill"),
Study3 = "Diseased", Study4 = "ill")
phenoControls <- list(Study1 = "Healthy", Study2 = c("Healthy", "control"),
Study3 = "Healthy", Study4 = "control")
newObjectMA <- createObjectMA(listEX = listMatrixEX,
listPheno = listPhenodatas,
namePheno = phenoGroups,
expGroups = phenoCases,
refGroups = phenoControls)
# Harmonize gene IDs
newObjectMA <- allSameID(newObjectMA, finalID = "GeneSymbol", organism = "Homo sapiens")
# Log-transform data
newObjectMA <- dataLog(newObjectMA)
# Test for heterogeneity
heterogeneityTest(newObjectMA)
# Perform meta-analysis
resultsMA <- metaAnalysisDE(newObjectMA, typeMethod = "REM", missAllow = 0.3, proportionData = 0.50)
# Visualize results
makeHeatmap(objectMA = newObjectMA, resMA = resultsMA, scaling = "zscor",
regulation = "all", numSig = 40, fdrSig = 0.05, logFCSig = 1.5, show_rownames = TRUE)
Inputs are lists of expression matrices and phenodata; output is a meta-analysis results table and a heatmap of significant genes.
Detect and remove batch effects from individual datasets and calculate individual study effect sizes or p-values.
library(DExMA)
# Remove batch effects
corrected_study2 <- batchRemove(listMatrixEX$Study2, listPhenodatas$Study2,
formula = ~gender+race,
mainCov = "race", nameGroup = "condition")
# Calculate individual study effect sizes
effects <- calculateES(newObjectMA)
# Calculate individual study p-values
pvalues <- pvalueIndAnalysis(newObjectMA)
Inputs are expression matrices and phenodata; outputs are batch-corrected expression matrices, individual study effect sizes, and individual p-values.
Download public microarray datasets from NCBI GEO for meta-analysis.
library(DExMA)
# Download GEO datasets
GEOobjects <- c("GSE4588", "GSE10325")
# dataGEO <- downloadGEOData(GEOobjects)
Input is a vector of GEO accession IDs; output is a list of downloaded GEO datasets.
metaAnalysisDE.allSameID.missGenesImput.batchRemove.limma, DESeq2, or edgeR directly because DExMA is designed for multi-study meta-analysis.Rsubread because DExMA requires pre-normalized expression matrices.objectMA created via createObjectMA or elementObjectMA).dataLog for log-transformation).ExpressionSet objects."GeneSymbol") in allSameID."Homo sapiens") in allSameID."REM" for random effects model, "maxP" for p-value combination) in metaAnalysisDE.0.3): The maximum proportion of missing values allowed for a gene.0.50): The minimum proportion of datasets in which a gene must be present.allSameID before performing meta-analysis.dataLog to ensure all datasets are in log scale.heterogeneityTest to decide between fixed-effects and random-effects models.missGenesImput to impute missing genes if you want to avoid discarding genes that are unmeasured in a subset of studies.dataLog to automatically detect and log-transform non-log datasets.missAllow and proportionData in metaAnalysisDE, or use missGenesImput to impute missing values.phenoCases and phenoControls lists when calling createObjectMA.limma for single-study differential expression and batch correction.swamp for principal component analysis and batch effect identification (e.g., prince).Biobase for managing ExpressionSet objects.まだレビューはありません。使ってみた感想をお寄せください。
概要と使いどころ
The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
日本語の概要は準備中です。原文の説明を表示しています。
This tool uses the label-tree function from HyPhy to annotate a phylogenetic tree. It allows users to select a subset of leaves using either a regular expression or a list of sequence names, and then apply a specified label to these selecte
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This package provides a client for the Bioconductor AnnotationHub web resource. The AnnotationHub web resource provides a central location where genomic files (e.g., VCF, bed, wig) and other resources from standard locations (e.g., UCSC, En
日本語の概要は準備中です。原文の説明を表示しています。
apeglm provides Bayesian shrinkage estimators for effect sizes for a variety of GLM models, using approximation of the posterior for individual coefficients.
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ASURAT is a software for single-cell data analysis. Using ASURAT, one can simultaneously perform unsupervised clustering and biological interpretation in terms of cell type, disease, biological process, and signaling pathway activity. Inputting a single-cell RNA-seq data and knowledge-based databases, such as Cell Ontology, Gene Ontology, KEGG, etc., ASURAT transforms gene expression tables into original multivariate tables, termed sign-by-sample matrices (SSMs).
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AUCell allows to identify cells with active gene sets (e.g. signatures, gene modules...) in single-cell RNA-seq data. AUCell uses the "Area Under the Curve" (AUC) to calculate whether a critical subset of the input gene set is enriched with
日本語の概要は準備中です。原文の説明を表示しています。