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ncborcherding avatar ncborcherding commented on August 21, 2024

Hey Tom,

Interesting idea - do you have an example of what you have in mind?

Thanks,
Nick

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tomthomas3000 avatar tomthomas3000 commented on August 21, 2024

For ex: out of a set of 20 genes supplied to the enrichit function, perhaps only 4-5 genes play an overwhelmingly important role in the enrichit score output. If this was the case, would it be possible identify the relative contribution of the individual genes to the score?

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daccachejoe avatar daccachejoe commented on August 21, 2024

hi - I am also wondering this. Any updates?

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ncborcherding avatar ncborcherding commented on August 21, 2024

Hey thanks for the question - working on a major overhaul of the package that will have the enrichment plot function. I do not have a timeline yet though.

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ncborcherding avatar ncborcherding commented on August 21, 2024

This took quite awhile (actually a lot harder than I thought), but the newest dev version of escape has enrichmentPlot() a function to examine the distribution of ranked gene order across single-cell groups.

https://ncborcherding.github.io/vignettes/escape_vignette.html#55_6_Enrichment_Plots

As of right now it just shows the mean rank across the group - I will work on adding the enrichment score and p-value calculation directly to the plot.

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tomthomas3000 avatar tomthomas3000 commented on August 21, 2024

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ncborcherding avatar ncborcherding commented on August 21, 2024

Hey Tom,

Absolutely - I think there are two approaches right now in the field for gene set for single-cell data, 1) pseudobulk and 2) true single-cell enrichment. There are some pluses/minuses to both approaches - I think pseudobulk produces more robust enrichment results for example. The calculation of enrichment at a single-cell level is probably better for the analysis of heterogeneity. You can use escape for either approach.

Let me know if you have any other questions.
Nick

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tomthomas3000 avatar tomthomas3000 commented on August 21, 2024

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ncborcherding avatar ncborcherding commented on August 21, 2024

Hey Tom,

Both the "ssGSEA" and the "UCell" method use raw count data. No need for normalization before running.

Nick

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