Entering edit mode
14 months ago
chunglee13
•
0
Dear all, I have a bulk RNA-seq dataset from a PBMC mixture that I want to deconvolute using the reference matrix from Monaco et al. However, I've noticed that only half of the genes in the Monaco reference matrix are present in my dataset. I used the AnnotationDbi package to compare Ensembl IDs between the two datasets.
- How can I improve or fix the gene matching issue between my bulk RNA-seq data and the Monaco reference matrix?
- How might these discrepancies affect the accuracy of the deconvolution using the CIBERSORT protocol?
- Are there any recommended strategies or tools to handle missing genes or improve the overlap?
Any insights or suggestions would be greatly appreciated!