Question

Zero pvalues after lfcShrink of DESeq2 package

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peibo_xu ▴ 10

@peibo_xu-15153

Last seen 5.6 years ago

Hi, I am using results by results() function from DESeq2 package to do volcano plot.

I found after I did lfcShrink function, I got many zero pvalues, but not before lfcShrink, even though I set independentFiltering=FALSE,cooksCutoff=FALSE.

How should I solve this? Any suggestion which one I should represent for a publication-ready plot?

deseq2 pvalue lfcshrink • 1.8k views

ADD COMMENT • link updated 5.6 years ago by Michael Love 42k • written 5.6 years ago by peibo_xu ▴ 10

score 0 · Answer 1 · 2019-03-30

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Michael Love 42k

@mikelove

Last seen 12 hours ago

United States

Please post your code. lfcShrink doesn’t computer pvalues, but just calls results() internally, so unless I can see your code I can’t help much. I find the shrunken LFC better for publication as the noisy LFC are removed in a data driven way.

ADD COMMENT • link 5.6 years ago Michael Love 42k

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Hi Michael, the user had posted a similar question as an issue to my EnhancedVolcano Bioconductor package: https://github.com/kevinblighe/EnhancedVolcano/issues/14

I forwarded them here in relation to their query about lfcshrink.

ADD REPLY • link 5.6 years ago Kevin Blighe ★ 4.0k

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Also see this other question wrt zero pvalues

https://support.bioconductor.org/p/119574/#119575

ADD REPLY • link 5.6 years ago Michael Love 42k

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Hi Michael, Thanks for helping. First, I should re-edit the issue, I before lfcShrink, I can see volcano plot is more flat(some pvalues are large), but after lfcShrink, many gene points are on the middle part of plot(very small pvaluse but about zero fold changes).

After checking with https://support.bioconductor.org/p/119574/#119575 this question, and the answer posted by Kevin, I guess zero pvalues may be due to lfcShrink and machine-specific lowest value set by EnhancedVolcano

Here is the code I run

res=results(dds, contrast = c("cell", "type1", "type2"),independentFiltering=FALSE,cooksCutoff=FALSE)
res1=lfcShrink(dds,contrast=c("cell", "type1", "type2"),independentFiltering=FALSE,cooksCutoff=FALSE)
res2=lfcShrink(dds,contrast=c("cell", "type1", "type2"),independentFiltering=TRUE,cooksCutoff=TRUE)

So for me, shrunken LFC looks better, but I do not how to deal with gene points very small pvaluse but about zero fold changes, is this a 'volcano plot' related issue?

Sorry for the confusion at the first time.

ADD REPLY • link 5.6 years ago peibo_xu ▴ 10

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Hey peibo_xu, just to confirm the steps:

if EnhancedVolcano detects a p-value equal to 0, it will automatically convert these to the value of .Machine$double.xmin. On my computer, this value is:

.Machine$double.xmin
[1] 2.225074e-308

Obviously, this is necessary because one cannot plot the negative log10 of 0:

-log10(0)
[1] Inf

You have the option of converting these p-values of 0 to something else, prior to using EnhancedVolcano. For example, you may simply convert them (just for plotting) to a magnitude of 10 lower than the lowest non-zero p-value, as this quick example shows:

pvalues <- c(0, 0.01, 0.05, 0, 0.0002)

min(pvalues[pvalues > 0])
[1] 0.0002

min(pvalues[pvalues > 0]) * 10^-1
[1] 0.00002

Now convert (impute) the p-values of 0:

pImpute <- min(pvalues[pvalues > 0]) * 10^-1
pvalues[pvalues == 0] <- pImpute
pvalues
[1] 0.00002 0.01 0.05 0.00002 0.0002

ADD REPLY • link 5.6 years ago Kevin Blighe ★ 4.0k

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The LFC shrinkage tends to be more “strict” about evidence on the LFC than the null hypothesis test. You can use svalues instead of adjusted pvalues which will give a consistent picture, by setting svalue=TRUE. See the apeglm paper for motivation and details.

ADD REPLY • link 5.6 years ago Michael Love 42k