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。
SimBu can be used to simulate bulk RNA-seq datasets with known cell type fractions. You can either use your own single-cell study for the simulation or the sfaira database. Different pre-defined simulation scenarios exist, as are options to run custom simulations. Additionally, expression values can be adapted by adding an mRNA bias, which produces more biologically relevant simulations.
インストールする前に、エージェントに与えられる指示の中身を確認できます。
Simulate pseudo-bulk RNA-seq data from custom single-cell count matrices or Seurat objects with controlled cell-type fractions and mRNA bias scaling.
library(SimBu)
# Create toy data
counts <- Matrix::Matrix(matrix(stats::rpois(3e5, 5), ncol = 300), sparse = TRUE)
tpm <- Matrix::Matrix(matrix(stats::rpois(3e5, 5), ncol = 300), sparse = TRUE)
tpm <- Matrix::t(1e6 * Matrix::t(tpm) / Matrix::colSums(tpm))
colnames(counts) <- paste0("cell_", rep(1:300))
colnames(tpm) <- paste0("cell_", rep(1:300))
rownames(counts) <- paste0("gene_", rep(1:1000))
rownames(tpm) <- paste0("gene_", rep(1:1000))
annotation <- data.frame(
"ID" = paste0("cell_", rep(1:300)),
"cell_type" = c(rep("T cells CD4", 150), rep("T cells CD8", 150))
)
# 1. Merge datasets (Create and merge)
ds1 <- SimBu::dataset(annotation = annotation, count_matrix = counts, tpm_matrix = tpm, name = "test_dataset1")
ds2 <- SimBu::dataset(annotation = annotation, count_matrix = counts, tpm_matrix = tpm, name = "test_dataset2")
ds_merged <- SimBu::dataset_merge(dataset_list = list(ds1, ds2), name = "merged_dataset")
# 2. Simulate pseudo-bulk samples
simulation1 <- SimBu::simulate_bulk(
data = ds_merged,
scenario = "random",
scaling_factor = "NONE",
ncells = 100,
nsamples = 10
)
simulation2 <- SimBu::simulate_bulk(
data = ds_merged,
scenario = "even",
scaling_factor = "NONE",
ncells = 100,
nsamples = 10
)
# 3. Merge simulations
merged_simulations <- SimBu::merge_simulations(list(simulation1, simulation2))
# 4. Plot the simulation results
SimBu::plot_simulation(simulation = merged_simulations)
Input: Single-cell count matrices and cell type annotations; Output: Simulated pseudo-bulk expression matrices and cell type fraction tables.
SimBu::simulate_bulk().scaling_factor parameter in SimBu::simulate_bulk().SimBu::dataset_seurat() or merging multiple datasets using SimBu::dataset_merge().EPIC or quanTIseq because SimBu is a simulation tool, not an estimator.spatialDE because SimBu is designed for bulk RNA-seq simulation from single-cell profiles.ID (matching matrix column names) and cell_type columns.SimBu::dataset() or SimBu::dataset_seurat().SimBu::dataset() to generate both count-based and TPM-based pseudo-bulk simulations.filter_genes = TRUE during dataset creation.SimBu::dataset().Seurat: For general single-cell preprocessing and analysis rather than pseudo-bulk simulation.scater: For single-cell quality control and visualization.scran: For single-cell normalization and variance modeling.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).
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。
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。