DESeq2 with interest only for 1 gene
4
0
Entering edit mode
fischer87 • 0
@fischer87-10933
Last seen 8.4 years ago

Hi everybody,
for a research, I  measured the expression levels of about 150 genes in 30 patients. Now, I'm interested to see if there is a difference, among three groups of these patients, in the expression levels of a particular gene (only one).

Could I use DESeq2 to do that?
The problem is that I can't use a statistical model directly on the raw data, then I would firstly normalize the raw data of this gene, secondly I want to do a correct statistical test.

I thought to use DEseq2 to normalize my gene using all the 150 genes, then do DESeq2 analysis and finally extract only the result for that gene (ignoring the others).

In your opinion, is it a correct procedures to do?

Thank you very much for your help, and sorry if my english is not correct, but I do not speak it very well.

Thank you again!
Bye

 

R deseq2 differential gene expression help • 2.2k views
ADD COMMENT
0
Entering edit mode
@mikelove
Last seen 1 hour ago
United States

Are there genes in the 150 that you expect to be not differentially expressed? If not, was there any external control (spike-in) included in the sequencing of each sample?

ADD COMMENT
0
Entering edit mode
fischer87 • 0
@fischer87-10933
Last seen 8.4 years ago

Yes, I expect that all the other 149 genes are not differentially expressed. I thought to leave all the 150 genes in the analysis in order to correctly normalize my gene of interest.

Sorry, how can I see the normalized counts? Is it correct to use the command:

dds <- DESeqDataSetFromMatrix(countData=countD, colData=colData, design=~condition)

NormData <- counts(dds, normalized=TRUE)

 

Thank you very much!

ADD COMMENT
0
Entering edit mode

(Note that if you are replying to my answer, you can use the Add Comment/Reply buttons instead of the Add Answer. Add Answer is for answering the top post, which is your own.(

Then you can just run DESeq() as normal. The 149 other genes should be sufficient to normalize the data, because the library size estimation is robust to a fraction of DE genes (just not when DE is the majority). I'd recommend using fitType="mean" when you have ~100 rows instead of the typical 1000s of rows in the DESeqDataSet.

Yes that is how you get normalized counts.

ADD REPLY
0
Entering edit mode
jshouse ▴ 10
@jshouse-10956
Last seen 23 months ago
United States

@fischer87  That is how I get normalized counts from DESeq2.

ADD COMMENT
0
Entering edit mode
fischer87 • 0
@fischer87-10933
Last seen 8.4 years ago

Thank you very much!!

ADD COMMENT
0
Entering edit mode

For future reference: these type of responses should be added as a comment to the answer you are replying to, which you can do by clicking on the big "ADD COMMENT" link below the text of every answer.

ADD REPLY
0
Entering edit mode

Sorry!

Thank you very much for your advice, surely in the future i will do that!

Bye

ADD REPLY

Login before adding your answer.

Traffic: 788 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6