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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This package performs differential pattern analysis for Ribo-seq data. It identifies genes with significantly different patterns in the ribosome footprint between two conditions. RiboDiPA contains five major components including bam file processing, P-site mapping, data binning, differential pattern analysis and footprint visualization.
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Run the entire RiboDiPA pipeline using the single wrapper function with default parameters.
library(RiboDiPA)
# Setup class label
classlabel <- data.frame(
condition = c("mutant", "mutant", "wildtype", "wildtype"),
comparison = c(2, 2, 1, 1)
)
rownames(classlabel) <- c("mutant1", "mutant2", "wildtype1", "wildtype2")
# Run wrapper
result.wrp <- RiboDiPA(
bam_path[1:4],
bam_path[5],
classlabel,
cores = 2
)
Note: Inputs are a vector of BAM file paths, a GTF file path, and a class label data frame; the output is a list containing gene-level test results and intermediate data.
This package performs differential pattern analysis for Ribo-seq data. It identifies genes with sign
Steps:
library(RiboDiPA)
# 1. Input File Verification and Setup (P-site mapping & Data binning)
data.psite <- psiteMapping(
bam_file_list = bam_path[1:4],
gtf_file = bam_path[5],
psite.mapping = "auto",
cores = 2
)
data.binned <- dataBinning(
data = data.psite$coverage,
bin.width = 0,
zero.omit = FALSE,
bin.from.5UTR = TRUE,
cores = 2
)
# 2. Save Results and Generate Plots (Differential pattern analysis & Plotting)
result.pst <- diffPatternTest(
data = data.binned,
classlabel = classlabel,
method = c('gtxr', 'qvalue')
)
plotTrack(data = data.psite, genes.list = c("YDR050C"), replicates = NULL, exons = FALSE)
Note: Inputs are BAM files, GTF file, and class label; the output is gene-level and bin-level differential pattern test results and footprint plots.
Perform differential pattern analysis using annotated exons as the bins for statistical testing.
library(RiboDiPA)
# P-site mapping
data.psite <- psiteMapping(
bam_file_list = bam_path[1:4],
gtf_file = bam_path[5],
psite.mapping = "auto",
cores = 2
)
# Exon-level binning and testing
result.exon <- diffPatternTestExon(
psitemap = data.psite,
classlabel = classlabel,
method = c('gtxr', 'qvalue')
)
Note: Inputs are P-site mapped data and class label; the output is exon-level differential pattern test results.
This package performs differential pattern analysis for Ribo-seq data. It identifies genes with sign
Steps:
library(RiboDiPA)
# 1. Retrieve User Input Files (P-site mapping)
data.psite <- psiteMapping(
bam_file_list = bam_path[1:4],
gtf_file = bam_path[5],
psite.mapping = "auto",
cores = 2
)
# 2. Define Experimental Design (Class Label) & Run exon-level test
result.exon <- diffPatternTestExon(
psitemap = data.psite,
classlabel = classlabel,
method = c('gtxr', 'qvalue')
)
# 3. Save Outputs and Generate Plots
plotTest(result = result.exon, genes.list = NULL, threshold = 0.05)
Note: Inputs are P-site mapped data and class label; the output is exon-level differential pattern test results and binned footprint plots.
RiboDiPA() or diffPatternTest().psiteMapping().dataBinning().diffPatternTestExon().plotTrack() and plotTest().igvR using bpTrack(), binTrack(), and exonTrack().DESeq2, edgeR, or limma instead.condition and comparison)."auto"): Rule for mapping RPFs to P-sites; can be "auto", "center", or a user-specified matrix of offsets.0): Width of bins in codons. 0 indicates adaptive binning.FALSE): If TRUE, bins with zero counts across all replicates are omitted from testing.TRUE): If TRUE, binning starts from the 5' end of the total transcript.c('gtxr', 'qvalue')): Methods for multiple comparison correction at the bin-level (e.g., 'gtxr') and gene-level (e.g., 'qvalue').0.05): Significance threshold for plotting or selecting genes.bin.width = 0) for sparse Ribo-seq datasets to optimize statistical power.cores parameter to speed up computationally intensive P-site mapping.psite.mapping = "center" or providing a custom offset matrix.DESeq2 for standard differential expression analysis of count data.edgeR for differential expression analysis using empirical Bayes methods.limma for linear modeling of gene expression data.아직 리뷰가 없습니다. 사용해 본 소감을 남겨 주세요.
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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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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
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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
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