DEG by deseq2 by Race
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Sharif • 0
@0f70ccd9
Last seen 8 months ago
United States

Hi Mike and community,

I am recently doing DEG analysis by using Deseq2. I am trying to get differentially expressed genes in African American (AAM) and European American (EAM) prostate cancer populations by using the TCGA dataset. My target is to see upregulated and downregulated genes in the African American population. I used the below code to set the level of my population.
As I want to see upregulated genes in African American Males (AAM), is it the right way to set the level? or I have to set the level as ("EAM", "AAM")?

sampledata$Race <- factor(sampledata$Race, levels=c("AAM", "EAM"))```


deseq2Data <- DESeqDataSetFromMatrix(countData=rawCounts_me, colData=sampleData_me, design= ~ Race)
DESeq2 • 321 views
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Kevin Blighe ★ 3.9k
@kevin
Last seen 7 days ago
Republic of Ireland

Hello,

Yes, by setting the levels of 'Race' in this way, AAM will be treated as the numerator and EAM as the denominator. Therefore, a gene with a positive fold-change will have higher expression in AAM compared to EAM.

Kind regards,

Kevin

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