In YosefLab/VISION: Functional interpretation of single cell RNA-seq latent manifolds

If you are already using Seurat for your analysis, VISION provides a convenience function for creating a Vision object from a Seurat object.

How this works

• By default, assay = "RNA", though this parameter is configurable.
• obj@[[assay]]@counts is used as the expression input (after normalizing to a library size of 10,000)
• The cell meta-data is taken from [e-mail]
• Lower-dimensional visualizations are taken each dimensionality reduction in Reductions(obj)
• These are added using their original names prefixed with "Seurat_"
• If "pca" has been run, the latentSpace input is taken from its associated cell embeddings
• The dimRed parameter can be used to select a different dimensionality reduction for this
• The dimRedComponents can be used to limit the number of components used (Default: All components)
• Otherwise, VISION computes the latentSpace by running PCA internally

Recommendations when using Seurat IntegrateData

When using IntegrateData, a new assay is created called integrated.

We recommend creating your reduced-dimensional representation using this assay by running PCA in Seurat after IntegrateData.

Then create the Vision object, but use the default assay="RNA".

• The original (normalized) counts will be used as the expression input
• However, the integrated latent space will be used to create the neighbors graph

Why not use the integrated expression data? Typically this data only consists of a subset of the genes (e.g. 2000 highly-variable genes) and so is not ideal for matching genes in signatures.

Examples

Assuming you already have a Seurat object defined as seurat.obj, you can use it in this way:

signatures <- c("data/h.all.v5.2.symbols.gmt")

vision.obj <- Vision(seurat.obj, signatures = signatures)

vision.obj <- analyze(vision.obj)

viewResults(vision.obj)

The above call would take the "pca" dimensionality reduction from seurat.obj if it is defined. If you instead had run a Diffusion Map using Seurat and wanted to use that as your latent space, you could specify that like this:

vision.obj <- Vision(seurat.obj,
    signatures = signatures,
    dimRed <- "dm")

Any of the other Vision() constructor parameters can also be passed here. For example, if you wanted to enable microclustering with 5 cells per micropool:

vision.obj <- Vision(seurat.obj,
    signatures = signatures,
    pool = T, cellsPerPartition = 5
    )

By default, Vision will still run tSNE as part of the main analysis pipeline. You may wish to skip this if a visualization has already been run in Seurat. To instruction VISION to not run any additional visualization projections, set projection_methods = NULL like so:

vision.obj <- Vision(seurat.obj,
    signatures = signatures,
    projection_methods = NULL)

YosefLab/VISION documentation built on June 14, 2024, 5:27 p.m.