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I applied cNMF to analyze my scRNA-seq data, and I focused on two output files: gene_spectra_score.k_3.dt_0_1.txt and gene_spectra_tpm.k_3.dt_0_1.txt. According to the manual, these files should represent essentially the same information but on different scales (Z-score vs. TPM). However, I noticed a significant discrepancy between the top 50 genes from each file, with only 15 genes overlapping between them. I used the R code below to extract the top genes for each GEP. Could there be an issue with my approach?
##########################################
exprSet = read.table(file = "MC.Merge.gene_spectra_score.k_3.dt_0_1.txt", header = TRUE, sep = "\t")
OR
exprSet = read.table(file = "MC.Merge.gene_spectra_tpm.k_3.dt_0_1.txt", header = TRUE, sep = "\t")
exprSet = exprSet[,-1]
rownames(exprSet) = paste(rep("C", 3), seq(1, 3, 1), sep = "")
top_genes = apply(exprSet, 1, function(x){ names(sort(x, decreasing = TRUE))[1:50]})
###########################################
Additionally, I exported the counts file with only HVGs from Seurat before applying cNMF, assuming it would save computation time. Is this approach acceptable?
The text was updated successfully, but these errors were encountered:
Hi,
I applied cNMF to analyze my scRNA-seq data, and I focused on two output files: gene_spectra_score.k_3.dt_0_1.txt and gene_spectra_tpm.k_3.dt_0_1.txt. According to the manual, these files should represent essentially the same information but on different scales (Z-score vs. TPM). However, I noticed a significant discrepancy between the top 50 genes from each file, with only 15 genes overlapping between them. I used the R code below to extract the top genes for each GEP. Could there be an issue with my approach?
##########################################
exprSet = read.table(file = "MC.Merge.gene_spectra_score.k_3.dt_0_1.txt", header = TRUE, sep = "\t")
OR
exprSet = read.table(file = "MC.Merge.gene_spectra_tpm.k_3.dt_0_1.txt", header = TRUE, sep = "\t")
exprSet = exprSet[,-1]
rownames(exprSet) = paste(rep("C", 3), seq(1, 3, 1), sep = "")
top_genes = apply(exprSet, 1, function(x){ names(sort(x, decreasing = TRUE))[1:50]})
###########################################
Additionally, I exported the counts file with only HVGs from Seurat before applying cNMF, assuming it would save computation time. Is this approach acceptable?
The text was updated successfully, but these errors were encountered: