Differential gene expression
1
0
Entering edit mode
20 days ago
4732b159 • 0

Hi all, I am just a bit concerned about my data and trying to understand what that means, could I please get insights from experienced fellows? and thanks in advance! In a differential gene expression analysis can it be possible that the number of up regulated genes is zero while there are over 200 genes down regulated in a diseased tissue? I have checked my code and model multiple times it looks like all is good. Please let me know what you suggest? all the best!

DESEq2 Differential gene expression • 753 views
ADD COMMENT
0
Entering edit mode

Sure can, but one would need some plots, such as plotMA to have an idea.

ADD REPLY
0
Entering edit mode

thanks for your response :) could you elaborate how to interpret that then?

ADD REPLY
0
Entering edit mode

you could add them first here

ADD REPLY
0
Entering edit mode

So,[ plotMA(res, ylim=c(-2,2)] it looks like that enter image description here

ADD REPLY
0
Entering edit mode
20 days ago
OmnibusX ▴ 90

From my experience, this usually happens when I compare data from different studies, technology, or alignment tools. In these cases, the number of genes in the 2 groups is not equal, for example, in group 1, the technology can capture only 10k genes, while in group 2 the technology can capture 20k genes, during differential expression analysis, genes that are present in group 2 but not in group 1 may appear significantly downregulated. This could potentially skew your results toward downregulation. If you could provide more details about your samples, it would help in diagnosing the origin of this issue more precisely.

ADD COMMENT
0
Entering edit mode

Hi Thanks for your reply :), really appreciated! The data that I am analyzing is from the same experiment of bulk RNA and I have two samples; disease and control. I am particularly interested in what the difference are between the same part of the tissue of disease vs control. I hope is it clearer now. Would you expect in this case? Thanks!

ADD REPLY
0
Entering edit mode

In case you only have two samples, which method did you use for DEG analysis?

ADD REPLY
0
Entering edit mode

I used DESq2 and designed it as below:

count_data <- as.matrix(count_data)

dds _t<- DESeqDataSetFromMatrix(countData = round(count_data), colData = col_data, design= ~group)

dds <- DESeq(dds_t)

res <- results(dds, contrast=c("group","Disease","Control"))

extra info: The group column of col_data is a factor and consist of Disease or Control.

{{{all(colnames(count_data) %in% rownames(col_data) ==> TRUE }}}

Thanks so much!

ADD REPLY
0
Entering edit mode

Sorry that I might not help in this case, as for the statistical test, I think we need more samples in each group (at least three) for a significant result. Therefore, I can not conclude anything yet.

ADD REPLY
0
Entering edit mode

Yes I do have more than three samples in each group: disease and control samples, more than 14 samples actually!

ADD REPLY
0
Entering edit mode

I saw your MA plot and code. Everything looks fine. This outcome might be because the disease state is characterized by a general suppression of gene activity or specific pathways, rather than activating different pathways.

ADD REPLY

Login before adding your answer.

Traffic: 2245 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