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I also did not find the corresponding cell type label of TEA-seq, could the author explain how to get the labels?
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Hi there,
Thanks for the package.
The output of the pipeline produced FCS files and pdf of UMAP images.
I do aim to use these FCS files in other packages, such as Spectre package to analyse…
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Hello, I cloned the directory from github, and then installed as directed. The installation seemed to be successful.
![image](https://user-images.githubusercontent.com/52397280/60609488-a0251f80-9d76…
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Hi all,
first of all I am new to the analysis of flow cytometry data, but after playing around with some data I recognised that some events which fall right on the edges of a gate are considered wi…
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Hello Bioconductor team,
I am submitting my R package {staRgate} in consideration for Bioconductor release.
Thank you for your time and consideration!
Update the following URL to point to th…
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Hi,
When trying to run the following command with version 2.0.1
```
$BNG_DIR/runBNG denovo \
-t /BiO/Access/cdmm92/resource/bionano/tools/pipeline/Solve3.6.1_11162020/RefAligner/11442…
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This seems a silly question, but I really confused with why I get a half estimated compared to the tutorial with the same commands.
So I have followed https://github.com/KamilSJaron/smudgeplot/wiki…
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## 🚀 Feature
For tree-structured files, add a tree view to the napari UI for showing/hiding images.
Allow metadata-based, user-controlled grouping of layers to apply layer properties to groups o…
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Reviewer: Dav Clark
Department/Center/Division: D-Lab
Institution/University/Company: UC Berkeley
Field of interest / expertise: Computational Social Science / Neuroscience
Country: USA
Article revie…
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Dear Author,
Thanks for this new API.
As you mentioned in your paper, the paragraph of **Hierarchical optimization for highly correlated cell types**.
"we ran AutoGeneS separated CD4+ and CD8+ …