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Answer: discrepancy in IDs from file and tx2gene (IDs don't match)
by
James W. MacDonald
68k
I don't think there's an easy fix (depending on your definition of easy, which may vary from mine). Ideally the transcript IDs used for ali…
Answer: Best practice for handling large data (matrix with >2^31-1 non-zero elements) in
by
Aaron Lun
★ 28k
Consider using a `SVT_SparseMatrix` from the **SparseArray** package, which is explicitly designed for this. **DropletUtils** (in BioC-deve…
Comment: Regarding the issue of background genes in enrichment analysis
by
zalinkaelisa
• 0
Use good features to distinguish the situation of the type of experiment [baseball 9][1] [1]: https://baseball9.io/
Comment: Heatmap of the Count Matrix
by
gta5movilecom
• 0
Using it for the top 20 genes in the heatmap highlights high-expression genes, but may miss out on variance-driven patterns. If you want to…
Answer: Regarding the issue of background genes in enrichment analysis
by
ATpoint
★ 4.9k
It should imo be the genes that were eligable to yield a "significant" result in your analysis. So, if you test set is derived from differe…
Votes
Regarding the issue of background genes in enrichment analysis
Best practice for handling large data (matrix with >2^31-1 non-zero elements) in SingleCellExperiment?
Comment: How can I avoid artifacts in gene set/pathway scoring by UCell and similar algor
Answer: I would like to perform differential expression analysis of lncRNAs using DESeq2
I would like to perform differential expression analysis of lncRNAs using DESeq2 and edgeR.
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