Hey,
I want to analyze Differential Transcript Usage (DTU) for TCGA isoform/transcript expression data while taking GTEx as "normal" reference. In other words, TCGA "tumor" and GTEx "normal" samples will be compared.
In order to remove variation caused by batch effects, I have to perform some batch correction. Here is a subset of my design matrix:
X sample condition batch
- s1 tumor TCGA
- s2 tumor TCGA
- s3 tumor TCGA
- s4 normal GTEx
- s5 normal GTEx
- s6 normal GTEx
Following error is received when trying to run DEXSeq:
"The supplied design matrix will result in a model matrix that is not full rank"
I know that the error is received due to redundancy in my design matrix. But I want help in tackling this issue? Is there any way for me to modify my design matrix so as to avoid this error? Can I use TCGA and GTEx data without batch correction?
Your help will be much appreciated.
tcga
gtex
rna-seq
why not just use the normal TCGA sample from the same individual?
Firstly, the samples are that of "adjacent" tissues (of cancer patients) and not exactly "normal". Secondly, I want to see the differences at 3 levels (NAT, normal, tumor).