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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Use bioconductor-monocle to outline a reproducible pseudotime and differential-expression analysis for [single-cell expression dataset], including required cell and feature metadata.
Required inputs
[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.
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
This skill is the knowledge layer — when, why, and how to use monocle. To run this analysis on your own data with managed compute, automated QC, and reproducible outputs, use BioMate — free to start.