본문으로 건너뛰기
cccskills
무료GitHub에 공개

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

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

설치 방법 보기

포함된 파일(1)

  • SKILL.md5.6 KB

SKILL.md(원문)

설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.

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 →

리뷰

아직 리뷰가 없습니다. 사용해 본 소감을 남겨 주세요.

댓글

로그인 없이 쓸 수 있습니다. 사용 후기, 질문, 작동하지 않은 환경 등을 편하게 남겨 주세요.

아직 댓글이 없습니다. 첫 댓글을 남겨 보세요.

보내면 바로 공개됩니다. 이메일 주소나 전화번호 같은 개인 정보는 쓰지 마세요. URL은 2개까지입니다.

0 / 1,000자

이 양식은 reCAPTCHA로 보호되며 Google 개인정보처리방침 및 서비스 약관이 적용됩니다.

같은 저장소의 스킬

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.

bioMate-AI/biomate-bioconductor-kb7932026년 6월 21일 업데이트

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.

bioMate-AI/biomate-bioconductor-kb7932026년 6월 21일 업데이트

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.

bioMate-AI/biomate-bioconductor-kb7932026년 6월 21일 업데이트

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.

bioMate-AI/biomate-bioconductor-kb7932026년 6월 21일 업데이트

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.

bioMate-AI/biomate-bioconductor-kb7932026년 6월 21일 업데이트

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.

bioMate-AI/biomate-bioconductor-kb7932026년 6월 21일 업데이트

bioMate-AI의 스킬 모두 보기

이 스킬의 문제 신고