본문으로 건너뛰기
cccskills
무료GitHub에 공개

bioconductor-scdblfinder

The scDblFinder package gathers various methods for the detection and handling of doublets/multiplets in single-cell sequencing data (i.e. multiple cells captured within the same droplet or reaction volume). It includes methods formerly fou

한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.

설치 방법 보기

포함된 파일(1)

  • SKILL.md5.8 KB

SKILL.md(원문)

설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.

scDblFinder

Dependencies & Environment

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

  • Version: 1.26.0 · Bioconductor: 3.23 · R: ≥ 4.6
  • Depends: SingleCellExperiment
  • Imports: igraph, Matrix, BiocGenerics, BiocParallel, BiocNeighbors, BiocSingular, S4Vectors, SummarizedExperiment, scran, scater, scuttle, bluster, DelayedArray, xgboost, MASS, IRanges, GenomicRanges, GenomeInfoDb, Rsamtools, rtracklayer
  • Install: BiocManager::install("scDblFinder")

When to Use

  • Identifying heterotypic doublets in single-cell RNA sequencing data using the scDblFinder iterative classifier.
  • Detecting doublets in multiplexed samples by processing each capture separately using the samples argument.
  • Testing for specific doublet type enrichments (e.g., combinations of clusters) using doubletPairwiseEnrichment or clusterStickiness.
  • Recovering intra-sample doublets that are neighbors to known inter-sample doublets (e.g., from cell hashing) using recoverDoublets.

When NOT to Use

  • For identifying homotypic doublets or inter-sample doublets in multiplexed experiments (use cell hashing or genotype-based SNP calls instead, as scDblFinder focuses on transcriptionally distinct heterotypic doublets).

Data Requirements

  • A SingleCellExperiment object or a simple count matrix containing raw counts (assay 'counts').
  • Empty droplets should already be removed prior to running the tool.

Key Parameters

  • samples (NULL): Column name in colData or a vector indicating the sample/capture of origin to process batches separately.
  • clusters (FALSE): Cluster labels or TRUE to use fastcluster; enables cluster-based artificial doublet generation.
  • dbr (NULL): Expected proportion of doublets; if omitted, automatically estimated based on the number of captured cells.
  • dbr.per1k (0.008): Expected doublet rate per thousand cells, defaulting to standard 10X rates.
  • artificialDoublets (NULL): Number of artificial doublets to generate; defaults to roughly the number of cells.
  • nfeatures (1000): Number of top expressed genes to retain for dimensionality reduction to speed up analysis.

Best Practices

  • Always split multi-sample datasets by providing the samples argument so doublets are sought independently for each capture.
  • Use the cluster-based approach (clusters=TRUE) if your dataset has a very clear cluster structure to avoid generating unidentifiable homotypic artificial doublets.
  • Check the distribution of doublet scores (hist(sce$scDblFinder.score)); a bimodal distribution indicates successful doublet identification.
  • If running multiple samples with the cluster-based approach, pre-cluster all samples together using fastcluster and pass the labels to the clusters argument to ensure concordant labels across samples.

Common Pitfalls

  • Way too many doublets called: Often caused by pooling multiple samples without specifying the samples argument, making the tool assume a massive single capture. Fix: Provide the samples argument to split cells by capture/batch.
  • 'Size factors should be positive' error: Caused by cells with zero reads or very low read counts that drop to zero after feature selection. Fix: Filter out empty droplets and extremely low-count cells before running scDblFinder.
  • Nonsensical cluster labels across samples: When running multiple samples without providing cluster labels, scDblFinder clusters them sample-wise, leading to mismatched labels. Fix: Pre-cluster all samples together using fastcluster and pass the labels to the clusters argument.

Alternatives

  • computeDoubletDensity: A simpler density-based method (formerly scran::doubletCells) that identifies cells with a high local density of artificial doublets.
  • findDoubletClusters: Identifies entire clusters that are likely composed of doublets by checking if their expression profile lies between two other clusters.
  • directDblClassification: Trains a classifier directly on gene expression without the kNN step, though generally yields worse predictions than scDblFinder.

Citations

  • Germain, P. L., Lun, A., Macnair, W., & Robinson, M. D. (2021). Doublet identification in single-cell sequencing data using scDblFinder. F1000Research, 10, 979.
  • Howitt et al., 2024. (Referenced regarding doublets in 10x Flex datasets).

References

  • Homepage: bioconductor.org/packages/scDblFinder
  • Vignette: vignette_0_d20f7c0c.txt
<!-- biomate-cta -->

Run this on BioMate

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

▶ Open scdblfinder 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