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workflowinstall
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3.0k
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workflowInstall is not working
workflowinstall
workflows
7.1 years ago
mckf11111
• 0
2
votes
10
replies
2.5k
views
Trouble Installing lifOver workflow
software error
liftOver
workflowinstall
package installation
updated 8.2 years ago by
James W. MacDonald
67k • written 8.2 years ago by
JustGettinStarted
• 0
0
votes
1
reply
1.9k
views
can't install workflow "rnaseqGene" with Bioconductor version3.3
bioconductor
workflowinstall
error
rnaseqgene
updated 8.5 years ago by
Valerie Obenchain
★ 6.8k • written 8.5 years ago by
cagenet34
▴ 20
1
vote
2
replies
1.5k
views
Workflows in BioC 3.3
workflows
workflowinstall
3.3
8.6 years ago
Axel Klenk
★ 1.0k
0
votes
1
reply
1.6k
views
workflowInstall issues; missing Windows binary
software error
missing data
workflowinstall
9.6 years ago
anoll2
• 0
0
votes
3
replies
1.5k
views
workflowInstall issues with OS X 10.9-10.10
workflowinstall
updated 9.7 years ago by
Dan Tenenbaum
★ 8.2k • written 9.7 years ago by
jlb
• 0
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Answer: Limma - using both array and spot weights in lmFit
by
henty1308
• 0
[BitLife][1] characters can go to jail for crimes. Escape or reform to return to normal life. [1]: https://bitlife-game.io
Answer: Limma - using both array and spot weights in lmFit
by
Gordon Smyth
52k
Was answered here: https://support.bioconductor.org/p/17028/
Comment: Easiest way to convert read10xMolInfo data into a dataframe in R with gene label
by
daldabrown9
• 0
For more info visit us on [R350 status check][1] [1]: https://sassagrantstatuscheck.co.za/
Answer: Margins for gene_set_enrichment_plot
by
Leonardo Collado Torres
★ 1.1k
Hi, In version 1.19.4 of `spatialLIBD` @lahuuki re-implemented the `gene_set_enrichment_plot()` function using `ComplexHeatmap::Heatmap(…
Comment: miRTarRnaseq library
by
mercedeh.movassagh
▴ 20
Maria please read the mirTarRnaSeq paper. In particular, Supplemental Table 2, clarifies all the statistical models, inputs and outputs. If…
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Answer: Fold change calculation in Diffbind vs. DESEQ2?
Fold change calculation in Diffbind vs. DESEQ2?
FeatureCounts Output Counts at Exon Level Using Default Settings, want gene level
Answer: FeatureCounts Output Counts at Exon Level Using Default Settings, want gene leve
Whether to build DESeq2 model with all data and then contrast groups or subset groups first, build model and then contrast?
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