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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SpatialDE is a method to find spatially variable genes (SVG) from spatial transcriptomics data. This package provides wrappers to use the Python SpatialDE library in R, using reticulate and basilisk.
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Identify, classify, and cluster spatially variable genes from raw count matrices and spatial coordinates.
library(spatialDE)
library(ggplot2)
# Load data
data("Rep11_MOB_0")
data("MOB_sample_info")
# 1. Filter out unobserved genes and calculate total counts per spot
counts <- Rep11_MOB_0[rowSums(Rep11_MOB_0) >= 3, ]
counts <- counts[, row.names(MOB_sample_info)]
MOB_sample_info$total_counts <- colSums(counts)
X <- MOB_sample_info[, c("x", "y")]
# 2. Stabilize variance using Anscombe's approximation
norm_expr <- stabilize(counts)
# 3. Regress out library size effects
resid_expr <- regress_out(norm_expr, sample_info = MOB_sample_info)
# 4. Classify SVGs into interpretable classes
sample_resid_expr <- head(resid_expr, 1000)
results <- spatialDE::run(sample_resid_expr, coordinates = X)
de_results <- results[results$qval < 0.05, ]
ms_results <- model_search(sample_resid_expr, coordinates = X, de_results = de_results)
# 5. Group SVGs into spatial patterns
sp <- spatial_patterns(sample_resid_expr, coordinates = X, de_results = de_results, n_patterns = 4L, length = 1.5)
# 6. Visualize results
FSV_sig(results, ms_results)
Input: Raw count matrices and spatial coordinates; Output: Spatially variable gene tables, model classifications, and spatial pattern clusters.
Identify, classify, and cluster spatially variable genes directly using a SpatialExperiment object.
library(spatialDE)
library(SpatialExperiment)
# Load data
data("Rep11_MOB_0")
data("MOB_sample_info")
partial_counts <- head(Rep11_MOB_0, 1000)
spe <- SpatialExperiment(
assays = list(counts = partial_counts),
spatialData = DataFrame(MOB_sample_info[, c("x", "y")]),
spatialCoordsNames = c("x", "y")
)
# Run spatialDE on SpatialExperiment
out <- spatialDE(spe, assay_type = "counts", verbose = FALSE)
# 1. Visualize spatial patterns of multiple genes
spe_results <- out[out$qval < 0.05, ]
ordered_spe_results <- spe_results[order(spe_results$qval), ]
multiGenePlots(spe, assay_type = "counts", ordered_spe_results[1:6, ]$g, point_size = 4, viridis_option = "D", dark_theme = FALSE)
# 2. Classify SVGs into interpretable classes
msearch <- modelSearch(spe, de_results = out, qval_thresh = 0.05, verbose = FALSE)
# 3. Group SVGs into spatial patterns
spatterns <- spatialPatterns(spe, de_results = spe_results, qval_thresh = 0.05, n_patterns = 4L, length = 1.5, verbose = FALSE)
Input: A SpatialExperiment object; Output: Updated data frames of spatially variable genes, model classifications, and spatial patterns.
spatialDE::run() or spatialDE().stabilize().regress_out().model_search() or modelSearch().spatial_patterns() or spatialPatterns().scran or DESeq2 because spatialDE requires spatial coordinates.BayesSpace because spatialDE focuses on identifying and clustering spatially variable genes.SpatialExperiment object.x and y) of the spots.spatialDE::run().modelSearch() or spatialPatterns().SpatialExperiment workflows.rowSums(counts) >= 3) before running the pipeline to reduce computational overhead.stabilize() and regress out library size effects using regress_out() before running the core SpatialDE test.stabilize() first.stabilize() expects samples in columns and genes in rows, whereas SpatialExperiment objects store genes in rows and spots in columns; ensure correct orientation or use the SpatialExperiment wrapper spatialDE().SpatialExperiment: For storing and manipulating spatial transcriptomics data.ggplot2: For custom spatial gene expression plotting.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
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 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.
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。
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。