The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Variance-stabilizing transformations help with the analysis of heteroskedastic data (i.e., data where the variance is not constant, like count data). This package provide two types of variance stabilizing transformations: (1) methods based on the delta method (e.g., 'acosh', 'log(x+1)'), (2) model residual based (Pearson and randomized quantile residuals).
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
Apply delta method-based transformations (acosh or shifted logarithm) to stabilize the variance of count data.
library(transformGamPoi)
library(SingleCellExperiment)
# Load the data
sce <- TENxPBMCData::TENxPBMCData("pbmc4k")
sce <- sce[sample(nrow(sce), 1000), sample(ncol(sce), 500)]
# Apply the acosh transformation to the count matrix
assay(sce, "acosh") <- acosh_transform(assay(sce, "counts"))
# Alternatively, apply the shifted log transformation with a specified pseudo-count
y_shiftLog <- shifted_log_transform(assay(sce, "counts"), pseudo_count = 1/(4 * 0.1))
Inputs are a SingleCellExperiment or count matrix; outputs are variance-stabilized values added as an assay or returned as a matrix.
Apply model residuals-based transformations (Pearson or randomized quantile residuals) to stabilize variance across all genes, including lowly expressed ones.
library(transformGamPoi)
library(SingleCellExperiment)
# Load the data
sce <- TENxPBMCData::TENxPBMCData("pbmc4k")
sce <- sce[sample(nrow(sce), 1000), sample(ncol(sce), 500)]
# Apply the Pearson residuals transformation with clipping
assay(sce, "pearson") <- residual_transform(sce, "pearson", clipping = TRUE, on_disk = FALSE)
# Alternatively, apply the randomized quantile residuals transformation
assay(sce, "rand_quantile") <- residual_transform(sce, "randomized_quantile", on_disk = FALSE)
Inputs are a SingleCellExperiment or count matrix; outputs are Pearson or randomized quantile residuals.
residual_transform).glmGamPoi or DESeq2 which model the count distribution directly.matrix, dgCMatrix, DelayedArray, SummarizedExperiment, SingleCellExperiment).rowMeans2(counts(sce)) > 0).acosh_transform.shifted_log_transform.residual_transform.residual_transform.rowMeans2 before applying transformations.acosh_transform or shifted_log_transform to retain sparsity of the input data (ensuring $g(0) = 0$).residual_transform with "randomized_quantile") to handle the discrete nature of counts and stabilize variance for lowly expressed genes.shifted_log_transform or acosh_transform which are designed to preserve sparsity ($g(0) = 0$).acosh) still show increasing variance for low mean expression ($\mu < 0.5$). Fix: Use residual_transform with Pearson or randomized quantile residuals instead.scry: For deviance residuals as a feature selection and dimension reduction tool.sctransform (Seurat): For regularized negative binomial regression-based normalization.scran: For pooling-based size factor normalization.아직 리뷰가 없습니다. 사용해 본 소감을 남겨 주세요.
로그인 없이 쓸 수 있습니다. 사용 후기, 질문, 작동하지 않은 환경 등을 편하게 남겨 주세요.
아직 댓글이 없습니다. 첫 댓글을 남겨 보세요.
The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
apeglm provides Bayesian shrinkage estimators for effect sizes for a variety of GLM models, using approximation of the posterior for individual coefficients.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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).
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.