本文へ移動
cccskills
無料GitHub で公開

bioconductor-gsva

Gene Set Variation Analysis (GSVA) is a non-parametric, unsupervised method for estimating variation of gene set enrichment through the samples of a expression data set. GSVA performs a change in coordinate systems, transforming the data fr

インストール方法を見る

含まれるファイル(1)

  • SKILL.md5.6 KB

SKILL.md(原文)

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。

GSVA

Dependencies & Environment

Package-intrinsic requirements from the Bioconductor landing page — reproduce in any R environment.

  • Version: 2.6.2 · Bioconductor: 3.23 · R: ≥ 4.6
  • Imports: BiocGenerics, MatrixGenerics, S4Vectors, S4Arrays, HDF5Array, SparseArray, DelayedArray, IRanges, Biobase, SummarizedExperiment, GSEABase, Matrix, DelayedMatrixStats, BiocParallel, SingleCellExperiment, BiocSingular, SpatialExperiment, sparseMatrixStats, cli, memuse
  • Install: BiocManager::install("GSVA")

When to Use

  • Sample-Wise Pathway Scoring: Calculating sample-specific pathway enrichment scores from a gene expression matrix using gsva.
  • Dimensionality Reduction: Transforming a high-dimensional gene-by-sample matrix into a lower-dimensional pathway-by-sample matrix for downstream analysis.
  • Method-Specific Enrichment: Applying specific single-sample enrichment methods like PLAGE, z-score, or ssGSEA using plageParam, zscoreParam, or ssgseaParam.

When NOT to Use

  • For Simple Differential Expression: For simple differential expression of individual genes, use edgeR because it is designed for gene-level count data modeling rather than gene set enrichment.
  • For Purely Managing Gene Sets: For purely importing and managing gene set collections without analysis, use GSEABase because it provides dedicated classes like GeneSetCollection and functions like getGmt.

Data Requirements

  • Expression Matrix: A normalized gene expression matrix, an ExpressionSet, or a SummarizedExperiment object.
  • Gene Sets: A list object of gene identifiers or a GeneSetCollection object.

Key Parameters

  • kcdf ("auto"): Kernel consensus density estimation; use "Gaussian" for continuous data or "Poisson" for integer counts.
  • kcdfNoneMinSampleSize (200): Minimum sample size at which the empirical cumulative distribution function is estimated directly without a kernel.
  • tau (1): Exponent defining the weight of the tail in the random walk.
  • maxDiff (TRUE): Logical flag specifying whether to calculate the enrichment score as the magnitude difference between the largest positive and negative random walk deviations.
  • absRanking (FALSE): Logical flag implying whether a modified Kuiper statistic is used.
  • sparse (FALSE): Logical flag used when the input expression data is stored in a sparse matrix.
  • minSize (1): Minimum size of gene sets to be considered.
  • maxSize (Inf): Maximum size of gene sets to be considered.

Best Practices

  • Match Identifiers: Ensure gene identifiers between the expression data matrix and the gene sets belong to the same standard nomenclature to allow mapIdentifiers to work.
  • Set the Correct Kernel: Use kcdf="Poisson" when providing RNA-seq integer count data directly to gsvaParam.
  • Import GMTs Safely: Use readGMT to import gene sets from GMT files, as it handles duplicated gene set names better than base R functions.

Common Pitfalls

  • Providing Raw Counts with Gaussian Kernel: Running GSVA on raw RNA-seq counts without changing the kernel. Fix: Set kcdf="Poisson" in gsvaParam when using integer counts.
  • Identifier Mismatch: Gene identifiers do not match between the expression matrix and gene sets. Fix: Provide data using specialized containers (like ExpressionSet or SummarizedExperiment) so GSVA can automatically map identifiers.
  • Duplicated Gene Set Names: Duplicated gene set names in GMT files causing errors with standard import functions. Fix: Use the readGMT function which deduplicates gene set names by default.

Alternatives

  • GSEABase: For foundational gene set data structures and basic GMT file importing.
  • qusage: Provides alternative functions like read.gmt for reading gene sets.
  • edgeR: For gene-level differential expression analysis using log-CPM units.

Citations

  • Hänzelmann S, Castelo R, Guinney J. "GSVA: gene set variation analysis for microarray and RNA-seq data." BMC Bioinformatics, 2013.
  • Barbie et al. "Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1." Nature, 2009.

References

<!-- biomate-cta -->

Run this on BioMate

This skill is the knowledge layer — when, why, and how to use gsva. To run this analysis on your own data with managed compute, automated QC, and reproducible outputs, use BioMate — free to start.

▶ Open gsva on BioMate →

レビュー

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。

同じリポジトリのスキル

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。

bioMate-AI/biomate-bioconductor-kb8042026年6月21日 更新

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。

bioMate-AI/biomate-bioconductor-kb8042026年6月21日 更新

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。

bioMate-AI/biomate-bioconductor-kb8042026年6月21日 更新

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。

bioMate-AI/biomate-bioconductor-kb8042026年6月21日 更新

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。

bioMate-AI/biomate-bioconductor-kb8042026年6月21日 更新

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。

bioMate-AI/biomate-bioconductor-kb8042026年6月21日 更新

bioMate-AI のスキルをすべて見る

このスキルの問題を報告する