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bioconductor-monocle

Monocle performs differential expression and time-series analysis for single-cell expression experiments. It orders individual cells according to progress through a biological process, without knowing ahead of time which genes define progre

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bioconductor-monocle

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Use bioconductor-monocle to outline a reproducible pseudotime and differential-expression analysis for [single-cell expression dataset], including required cell and feature metadata.

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  • [single-cell expression dataset]

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SKILL.md

name: bioconductor-monocledescription: Monocle performs differential expression and time-series analysis for single-cell expression experiments. It orders individual cells according to progress through a biological process, without knowing ahead of time which genes define progrewhen_to_use: "Use when: Analyzing single-cell RNA-Seq experiments to study complex biological processes.; Ordering single cells in pseudotime to place them along a trajectory corresponding to a biological process such as cell differentiation.; Performing differential gene expression and clustering to identify important genes and cell states.; Visualizing data distributions or trajectories using plot().. Not for: For bulk RNA-Seq differential expression, use DESeq2 instead because Monocle is specifically designed for single-cell RNA-Seq experiments.; For Python-based single-cell workflows, use Scanpy instead because Monocle is an R package."user-invocable: false

monocle

Dependencies & Environment

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

  • Version: 2.40.0 · Bioconductor: 3.23 · R: ≥ 4.6
  • Depends: Matrix, Biobase, ggplot2, VGAM, DDRTree
  • Imports: igraph, BiocGenerics, HSMMSingleCell, plyr, cluster, combinat, fastICA, irlba, matrixStats, Rtsne, MASS, reshape2, leidenbase, limma, tibble, dplyr, pheatmap, stringr, proxy, slam, viridis, biocViews, RANN, Rcpp
  • System requirements: URL
  • Install: BiocManager::install("monocle")

When to Use

  • Analyzing single-cell RNA-Seq experiments to study complex biological processes.
  • Ordering single cells in pseudotime to place them along a trajectory corresponding to a biological process such as cell differentiation.
  • Performing differential gene expression and clustering to identify important genes and cell states.
  • Visualizing data distributions or trajectories using plot().

When NOT to Use

  • For bulk RNA-Seq differential expression, use DESeq2 instead because Monocle is specifically designed for single-cell RNA-Seq experiments.
  • For Python-based single-cell workflows, use Scanpy instead because Monocle is an R package.

Data Requirements

  • Input Format: Single-cell gene expression data (e.g., RNA-Seq).
  • Structure: Expression matrices representing unsynchronized individual cells executing a gene expression program.

Key Parameters

  • warning (FALSE): Controls whether warnings are displayed during knitr chunk execution via opts_chunk$set().
  • dpi (600): Sets the resolution for generated plots via opts_chunk$set().
  • cache (FALSE): Controls whether to cache the knitr code chunks.

Best Practices

  • Load required prerequisite packages like Biobase, reshape2, and ggplot2 using library() before starting the analysis.
  • Use set.seed() to ensure reproducibility of the trajectory learning and clustering algorithms.
  • Configure global chunk options using opts_chunk$set() to ensure high-quality plot outputs.

Common Pitfalls

  • Missing Dependencies: Failing to load required packages will cause errors; fix this by running library(Biobase) and library(ggplot2) at the start of your script.
  • Non-Reproducible Results: Running the unsupervised trajectory algorithms without a seed can lead to variable results across runs; fix this by setting a random seed with set.seed().

Alternatives

  • monocle3: The completely redesigned successor to Monocle, optimized for large datasets and complex trajectories.
  • slingshot: A flexible, cluster-based trajectory inference tool for single-cell data.
  • scater: For upstream single-cell preprocessing, normalization, and quality control.

Citations

  • Trapnell C, Cacchiarelli D, et al. (2014). The dynamics and regulators of cell fate decisions are revealed by pseudo-temporal ordering of single cells. Nature Biotechnology, 32:381-386. PMID:24658644
  • Qiu X, Hill A, et al. (2017). Single-cell mRNA quantification and differential analysis with Census. Nature Methods, 14:309-315. PMID:28114287

References


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