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Reporting Tools
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DESeq2: Analyzing just two normal+tumour pairs
deseq2
reporting tools
6.0 years ago
mmokrejs
• 0
3
votes
7
replies
2.2k
views
ReportingTools Segmentation fault
reportingtools
reporting tools
updated 6.7 years ago by
becker.gabriel
▴ 10 • written 6.7 years ago by
michael
▴ 20
0
votes
0
replies
978
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Error with Reportingtools using ENSEMBL gene ID
reporting tools
modifyDF
survival
8.5 years ago
cagenet34
▴ 20
1
vote
4
replies
2.2k
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Reporting Tools error
Reporting Tools
updated 9.6 years ago by
Mayte Suarez-Farinas
▴ 510 • written 10.2 years ago by
Mayte
• 0
4 results • Page
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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…
Votes
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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