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# Submitting team
UI Team (Andy C.)
## SME
**Anath Shalev, MD**: Professor of Medicine – Endocrinology, Diabetes, and Metabolism, Department of Medicine; Director, Comprehensive Diabetes Cen…
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Hi all. I was looking through the `_rank_genes_groups` function and noticed that the fold-change calculations are based on the means calculated by `_get_mean_var`. The only problem with this is that (…
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**Question**
First of all, thank you for this wonderful tutorial! It has been immensely helpful in dealing with single-cell datasets, and I've gained valuable insights from it.
I've been struggl…
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Hi there! Thanks a lot for your package, it's really a great tool.
I have been using it for many years, but I recently came across some methodological discussion in relation to the methods of the G…
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Hello,
I can't find an example showing how to specify the 'reduction' parameter using the 'FindMarkers' function.
I have batch corrected my data using Harmony and would like to use its embeddings…
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Hi,
I have a few questions about the annotations provided by TEsmall.
The reads that are annotated as tRNA, are they tRFs? Or are they part of tRNA anticodons or both?
The reads that are annotated…
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Dear MaayanLab team,
Greetings, I hope this question finds you well.
Actually, it is neither reporting issues nor idea suggestions, I have a simple question about the data in the [here](https://ma…
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Hi Dear Seurat team,
I found mitochondrial genes exist in DEGs using FindAllMarkers in both Integrated and one or two subset celltype dataset, and they ranks top in DEGs. can I just remove mitochondr…
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Hi,
It's probably a really basic question here...
I understand how to use FindMarkers to find the DE genes between two conditions in my data.
However, I'm interested in finding out whether th…
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Dear Dr Cassan and authors.
This is the wonderful software and user interface that I have been looking for. This is a neat suite for differentially-expressed gene analysis yet I have an issue on the…