Draws a heatmap of single cell feature expression with cells ordered by their
mixscape ko probabilities.
object |
An object
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ident.1 |
Identity class to define markers for; pass an object of class
phylo or 'clustertree' to find markers for a node in a cluster tree;
passing 'clustertree' requires BuildClusterTree to have been run
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ident.2 |
A second identity class for comparison; if NULL ,
use all other cells for comparison; if an object of class phylo or
'clustertree' is passed to ident.1 , must pass a node to find markers for
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balanced |
Plot an equal number of genes with both groups of cells.
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logfc.threshold |
Limit testing to genes which show, on average, at least
X-fold difference (log-scale) between the two groups of cells. Default is 0.25.
Increasing logfc.threshold speeds up the function, but can miss weaker signals.
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assay |
Assay to use in differential expression testing
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max.genes |
Total number of DE genes to plot.
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test.use |
Denotes which test to use. Available options are:
"wilcox" : Identifies differentially expressed genes between two
groups of cells using a Wilcoxon Rank Sum test (default); will use a fast
implementation by Presto if installed
"wilcox_limma" : Identifies differentially expressed genes between two
groups of cells using the limma implementation of the Wilcoxon Rank Sum test;
set this option to reproduce results from Seurat v4
"bimod" : Likelihood-ratio test for single cell gene expression,
(McDavid et al., Bioinformatics, 2013)
"roc" : Identifies 'markers' of gene expression using ROC analysis.
For each gene, evaluates (using AUC) a classifier built on that gene alone,
to classify between two groups of cells. An AUC value of 1 means that
expression values for this gene alone can perfectly classify the two
groupings (i.e. Each of the cells in cells.1 exhibit a higher level than
each of the cells in cells.2). An AUC value of 0 also means there is perfect
classification, but in the other direction. A value of 0.5 implies that
the gene has no predictive power to classify the two groups. Returns a
'predictive power' (abs(AUC-0.5) * 2) ranked matrix of putative differentially
expressed genes.
"t" : Identify differentially expressed genes between two groups of
cells using the Student's t-test.
"negbinom" : Identifies differentially expressed genes between two
groups of cells using a negative binomial generalized linear model.
Use only for UMI-based datasets
"poisson" : Identifies differentially expressed genes between two
groups of cells using a poisson generalized linear model.
Use only for UMI-based datasets
"LR" : Uses a logistic regression framework to determine differentially
expressed genes. Constructs a logistic regression model predicting group
membership based on each feature individually and compares this to a null
model with a likelihood ratio test.
"MAST" : Identifies differentially expressed genes between two groups
of cells using a hurdle model tailored to scRNA-seq data. Utilizes the MAST
package to run the DE testing.
"DESeq2" : Identifies differentially expressed genes between two groups
of cells based on a model using DESeq2 which uses a negative binomial
distribution (Love et al, Genome Biology, 2014).This test does not support
pre-filtering of genes based on average difference (or percent detection rate)
between cell groups. However, genes may be pre-filtered based on their
minimum detection rate (min.pct) across both cell groups. To use this method,
please install DESeq2, using the instructions at
https://bioconductor.org/packages/release/bioc/html/DESeq2.html
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max.cells.group |
Number of cells per identity to plot.
|
order.by.prob |
Order cells on heatmap based on their mixscape knockout
probability from highest to lowest score.
|
group.by |
(Deprecated) Option to split densities based on mixscape
classification. Please use mixscape.class instead
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mixscape.class |
metadata column with mixscape classifications.
|
prtb.type |
specify type of CRISPR perturbation expected for labeling
mixscape classifications. Default is KO.
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fc.name |
Name of the fold change, average difference, or custom
function column in the output data.frame. Default is avg_log2FC
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pval.cutoff |
P-value cut-off for selection of significantly DE genes.
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... |
Arguments passed to other methods and to specific DE methods
|
A ggplot object.