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 is an advanced version of TDbasedUFE, which is a comprehensive package to perform Tensor decomposition based unsupervised feature extraction. In contrast to TDbasedUFE which can perform simple the feature selection and the multiomics analyses, this package can perform more complicated and advanced features, but they are not so popularly required. Only users who require more specific features can make use of its functionality.
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查看安装方法安装前可以查看交给 AI 代理的指令内容。
Integrate two omics datasets sharing the same features using memory-efficient SVD with partial summation.
library(TDbasedUFEadv)
library(RTCGA.rnaseq)
# Prepare drug and disease expression datasets
Cancer_cell_lines <- list(ACC.rnaseq, BLCA.rnaseq, BRCA.rnaseq, CESC.rnaseq)
Drug_and_Disease <- prepareexpDrugandDisease(Cancer_cell_lines)
expDrug <- Drug_and_Disease$expDrug
expDisease <- Drug_and_Disease$expDisease
# Compute SVD on the two matrices
SVD <- computeSVD(exprs(expDrug), exprs(expDisease))
# Generate the matrix product and prepare the tensor
Z <- t(exprs(expDrug)) %*% exprs(expDisease)
sample <- outer(
colnames(expDrug),
colnames(expDisease),
function(x, y) { paste(x, y) }
)
Z <- PrepareSummarizedExperimentTensor(
sample = sample,
feature = rownames(expDrug),
value = Z
)
Inputs are two expression matrices sharing features; output is a SummarizedExperiment-like tensor and SVD results.
Integrate multiple omics datasets sharing the same features but having different samples using projection-based SVD and HOSVD.
library(TDbasedUFEadv)
library(RTCGA.rnaseq)
library(RTCGA.clinical)
# Prepare a list of matrices sharing features
Multi <- list(
BLCA.rnaseq[seq_len(100), 1 + seq_len(1000)],
BRCA.rnaseq[seq_len(100), 1 + seq_len(1000)],
CESC.rnaseq[seq_len(100), 1 + seq_len(1000)],
COAD.rnaseq[seq_len(100), 1 + seq_len(1000)]
)
# Prepare a tensor from the list of matrices
Z <- prepareTensorfromList(Multi, 10L)
# Permute the tensor modes to align features
Z <- aperm(Z, c(2, 1, 3))
# Wrap the tensor using PrepareSummarizedExperimentTensor
Clinical <- list(BLCA.clinical, BRCA.clinical, CESC.clinical, COAD.clinical)
Multi_sample <- list(
BLCA.rnaseq[seq_len(100), 1, drop = FALSE],
BRCA.rnaseq[seq_len(100), 1, drop = FALSE],
CESC.rnaseq[seq_len(100), 1, drop = FALSE],
COAD.rnaseq[seq_len(100), 1, drop = FALSE]
)
ID_column_of_Multi_sample <- c(770, 1482, 773, 791)
ID_column_of_Clinical <- c(20, 20, 12, 14)
Z <- PrepareSummarizedExperimentTensor(
feature = colnames(ACC.rnaseq)[1 + seq_len(1000)],
sample = array("", 1),
value = Z,
sampleData = prepareCondTCGA(
Multi_sample,
Clinical,
ID_column_of_Multi_sample,
ID_column_of_Clinical
)
)
# Compute HOSVD
HOSVD <- computeHosvd(Z)
# Select features using selectFeatureProj in batch mode
cond <- attr(Z, "sampleData")
index <- selectFeatureProj(HOSVD, Multi, cond, de = 1e-3, input_all = 3)
# Extract and display selected features
head(tableFeatures(Z, index))
Inputs are a list of matrices sharing features and clinical metadata; output is a table of selected features with p-values.
Integrate multiple omics datasets sharing the same samples using projection-based SVD and HOSVD.
library(TDbasedUFEadv)
# Prepare a tensor from the list of matrices and wrap in a SummarizedExperiment-like object
# Z <- PrepareSummarizedExperimentTensor(sample = sample, feature = feature, value = value)
# Compute HOSVD
# HOSVD <- computeHosvd(Z)
# Select features across individual profiles
# index <- selectFeature(HOSVD, input_all, de = 0.05)
# Extract, print, and save selected features
# head(tableFeatures(Z, index))
Inputs are multi-omics matrices sharing samples; output is a table of selected features.
enrichR::enrichr, STRINGdb::STRINGdb, or DOSE::enrichDGN.DESeq2 or limma instead.SVD or HOSVD packages directly.RTCGA.rnaseq like BLCA.rnaseq).Multi) where rows represent features and columns represent samples.BLCA.clinical) to construct condition vectors for selecting singular value vectors.selectFeatureProj or selectFeature.selectSingularValueVectorLarge or selectFeatureProj.TDbasedUFE package workflows before moving to the advanced features of TDbasedUFEadv.computeSVD) when the number of features is too large to construct a full tensor.selectSingularValueVectorLarge.enrichR::enrichr or STRINGdb::STRINGdb to biologically validate the unsupervised feature selection.computeHosvd on a full tensor with too many features. Fix: Use computeSVD with partial summation to reduce memory requirements.aperm to permute the tensor modes appropriately before wrapping with PrepareSummarizedExperimentTensor.DESeq2: For supervised differential expression analysis.limma: For linear modeling of gene expression data.TDbasedUFE: For simpler, standard unsupervised feature extraction workflows.还没有评价。欢迎分享你的使用感受。
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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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