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cellcode
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cell analysis- significance output perturbed in shiny environment
cellcode
significance
9.0 years ago
christopher.clarskon15
▴ 20
1
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reply
2.2k
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CellMix compare results to CellCODE
cellmix
cellcode
updated 9.0 years ago by
Steve Lianoglou
★ 13k • written 9.0 years ago by
christopher.clarskon15
▴ 20
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1.6k
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reactive CellCODE heatmap
cellcode
shiny
heatmap
updated 9.0 years ago by
Andrzej Oleś
▴ 750 • written 9.0 years ago by
christopher.clarskon15
▴ 20
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1.7k
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CellCODE estimate cell proportions SPV analysis grouping comparisons faulty
CellCODE
differential gene expression
9.0 years ago
christopher.clarskon15
▴ 20
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Comment: How to left_join a tidySummarizedExperiment with a GRanges object by seqnames an
by
James W. MacDonald
68k
Have you figured out how to do this using tidy grammar? Using non-tidy grammar is quite simple, and perhaps you already know how to do that…
Comment: How can I correctly use phyloseq with Docker?
by
James W. MacDonald
68k
You can use [bioc-run][1] to simplify things as well. [1]: https://github.com/Bioconductor/bioc-run/tree/devel
Comment: How can I correctly use phyloseq with Docker?
by
James W. MacDonald
68k
You show how you modified the container, but not how you are running it, which is the critical part.
Comment: Discrepancies in normalised count data vs unnormalised
by
AMgroup
• 0
Thank you for your reply. > Per sample all counts are scaled by the same size factor so I strongly assume that something was parsed here …
Comment: Discrepancies in normalised count data vs unnormalised
by
ATpoint
★ 4.8k
Please show examples using `plotCounts()`. Custom spreadsheets harbor the risk of parsing errors along the way which very often explains wh…
Votes
Answer: How to combine two DESeq2 objects (dds) for analysis
How to combine two DESeq2 objects (dds) for analysis
How can I correctly use phyloseq with Docker?
A: DESeq2::sizeFactors() function does not output the sizeFactor table.
Comment: Filtering after DESeq
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