TreatDGE function usage
2
1
Entering edit mode
candida.vaz ▴ 50
@candidavaz-6923
Last seen 5.9 years ago
Singapore

Dear EDGER support team,

I have a single factor experiment with the 5 different samples having three replicates each.

group <- factor(c("a","a","a","b","b","b","c","c","c","d","d","d","e","e","e"))

Using a GLM based approach, and using TreatDGE function, I am trying to obtain the Differentially expressed genes. The following two kinds of comparisons are of interest to me:

1. (b vs a), (c vs a), (d vs a), (e vs a)

2. (c vs b), (e vs d)

For the 1st type of comparison, I was using this:

tr <- treatDGE(fit, coef=2, lfc=1) (b vs a)

tr <- treatDGE(fit, coef=3, lfc=1) (c vs a)

tr <- treatDGE(fit, coef=4, lfc=1) (d vs a)

tr <- treatDGE(fit, coef=5, lfc=1) (e vs a)

Is this correct?

How can I make use of the "contrast" argument of the TreatDGE function for these comparisons.

And how to do the second kind of comparisons? I read the TreatDGE function information provided, but not able to decide on how to use it correctly.

Thanks in advance for the help!

Candida

edger • 1.9k views
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3
Entering edit mode
@gordon-smyth
Last seen 58 minutes ago
WEHI, Melbourne, Australia

I'm assuming that your fit used the design matrix:

design <- model.matrix(~group)

To test (c vs b) you can use:

treatDGE(fit, contrast=c(0,-1,1,0,0), lfc=1)

To test (e vs d):

treatDGE(fit, contrast=c(0,0,0,-1,1), lfc=1)

Note that

treatDGE(fit, coef=2, lfc=1)

is just shorthand for:

treatDGE(fit, contrast=c(0,1,0,0,0), lfc=1)

In general, the contrast argument behaves the same for treatDGE() as it does for the glmLRT() function.

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0
Entering edit mode
candida.vaz ▴ 50
@candidavaz-6923
Last seen 5.9 years ago
Singapore

Dear Gordon,

Thanks a lot for your prompt reply,

I read in the edge R tutorial that "0+ in the model formula is an instruction not to include an intercept column and
instead to include a column for each group".

so I decided to fit my design matrix as: "design <- model.matrix(~0+group)"

x <- read.delim("known-miR-expression-profiling-max-read-counts.txt",row.names="Symbol")
group <- factor(c("a","a","a","b","b","b","c","c","c","d","d","d","e","e"))
y <- DGEList(counts=x,group=group)
data.frame(Sample=colnames(y),group)
y <- calcNormFactors(y)
norm.vals <- cpm(y)
design <- model.matrix(~0+group)
y <- estimateGLMCommonDisp(y, design, verbose=TRUE)
y <- estimateGLMTrendedDisp(y, design)
y <- estimateGLMTagwiseDisp(y, design)
fit <- glmFit(y, design)

for b vs a :

groupbvsgroupa <- makeContrasts(groupb-groupa, levels=design)
tr <- treatDGE(fit, contrast=groupbvsgroupa, lfc=1)

for c vs b :

groupcvsgroupb <- makeContrasts(groupc-groupb, levels=design)
tr <- treatDGE(fit, contrast=groupcvsgroupb, lfc=1)

Is this a correct way too?

Another doubt I had is that is one of the sample replicate is not good and I decide to remove it, so for 4 samples  (a-d)

I have 3 replicates and the 5th one (e) has two, can I still proceed as:

group <- factor(c("a","a","a","b","b","b","c","c","c","d","d","d","e","e"))

 

Thank you very much for your kind help!

Candida

 

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1
Entering edit mode

The specification of the contrasts looks good to me. Your code will still work without the problematic replicate from group E (though, whether or not it makes sense to remove that replicate is another matter). Make sure that you have also removed the corresponding column in the count matrix.

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0
Entering edit mode

Thanks Aaron,

Yes I have removed the corresponding column in the count matrix.

Thanks for the help!

Candida

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