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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A robust and outlier-aware method for testing differential tissue composition from single-cell data. This model can infer changes in tissue composition and heterogeneity, and can produce realistic data simulations based on any existing dataset. This model can also transfer knowledge from a large set of integrated datasets to increase accuracy further.
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Estimate and test differences in cell type composition across groups from single-cell count data, with optional outlier removal and visualization.
library(sccomp)
library(dplyr)
# Estimate composition and test differences with outlier removal
sccomp_result <- counts_obj |>
sccomp_estimate(
formula_composition = ~ type,
sample = "sample",
cell_group = "cell_group",
abundance = "count",
cores = 1,
verbose = FALSE
) |>
sccomp_remove_outliers(cores = 1, verbose = FALSE, max_sampling_iterations = 2000) |>
sccomp_test()
# Generate boxplot visualization
sccomp_result |> sccomp_boxplot(factor = "type")
Input: A count data frame or SingleCellExperiment/Seurat object. Output: A tibble containing composition effects, FDR, and outlier annotations.
Model and test differences in cell-group variability across groups.
library(sccomp)
# Estimate both composition and variability
res <- seurat_obj |>
sccomp_estimate(
formula_composition = ~ type,
formula_variability = ~ type,
sample = "sample",
cell_group = "cell_group",
cores = 1,
verbose = FALSE
)
# Test and plot credible intervals
plots <- res |> sccomp_test() |> plot()
plots$credible_intervals_1D
Input: A Seurat or SingleCellExperiment object. Output: A model fit with variability effects and 1D/2D credible interval plots.
Compare different composition models (e.g., with vs. without a covariate) using leave-one-out (loo) cross-validation.
library(sccomp)
library(loo)
# Fit model with factor association
model_with_factor_association <- seurat_obj |>
sccomp_estimate(
formula_composition = ~ type,
sample = "sample",
cell_group = "cell_group",
inference_method = "hmc",
enable_loo = TRUE,
verbose = FALSE
)
# Fit baseline model without association
model_without_association <- seurat_obj |>
sccomp_estimate(
formula_composition = ~ 1,
sample = "sample",
cell_group = "cell_group",
inference_method = "hmc",
enable_loo = TRUE,
verbose = FALSE
)
# Compare models using leave-one-out cross-validation
loo_compare(
attr(model_with_factor_association, "fit")$loo(),
attr(model_without_association, "fit")$loo()
)
Input: A Seurat or SingleCellExperiment object. Output: A comparison table containing elpd_diff and se_diff.
Model cell-type proportions with both fixed effects and random effects (e.g., random intercepts or random slopes).
library(sccomp)
# Fit a random intercept model
res <- seurat_obj |>
sccomp_estimate(
formula_composition = ~ type + (1 | group__),
sample = "sample",
cell_group = "cell_group",
bimodal_mean_variability_association = TRUE,
cores = 1,
verbose = FALSE
)
Input: A Seurat or SingleCellExperiment object with grouping variables in metadata. Output: A model fit containing fixed and random effect estimates.
sccomp_estimate).sccomp_remove_outliers).sccomp_estimate with formula_variability).DESeq2 or edgeR instead of sccomp which is designed for cell-type composition.abundance = "proportion") because it fails to model uncertainty for rare cell groups; use raw counts instead.Seurat object, SingleCellExperiment object, or a count tibble/data frame containing columns for sample, cell group, and abundance (counts).bimodal_mean_variability_association = TRUE. For CyTOF and microbiome data, set bimodal_mean_variability_association = FALSE.~ type).~ type)."count"): Column name representing counts or proportions.FALSE): Logical indicating whether to model bimodal mean-variability association (recommended TRUE for scRNA-seq).FALSE): Logical indicating whether to enable leave-one-out cross-validation."hcm"): Method used for inference (e.g., "hmc").sccomp_remove_outliers() when performing model comparison with loo_compare(), as leave-one-out cross-validation requires the models to be fit on the exact same data.plot_2D_intervals() or plots$credible_intervals_2D to ensure the linear association is satisfied before interpreting differential variability.sccomp_proportional_fold_change() to obtain intuitive proportional fold changes for communication, but rely on sccomp_test() for statistical significance.abundance = "count".loo_compare() to fail or be invalid because different numbers of data points may be removed. Fix: Omit sccomp_remove_outliers() when comparing models.scCODA: Uses a Dirichlet-multinomial model but does not model group-specific variability or outliers.propeller: Uses a logit-linear model with limma but does not model data count distribution directly.corncob: Uses a Beta-binomial model but does not support mixed-effect modeling or outlier detection.ANCOM-BC: Uses a log-linear model designed primarily for microbiome data.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。