Bioconductor Hugene10sttranscriptcluster.db annotation

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hugene10sttranscriptcluster.db annotation

6.2 years ago mengyuankan ▴ 20

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annotation hugene10sttranscriptcluster.db annotation

written 6.8 years ago by Ed Siefker ▴ 230

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bioconductor hugene10sttranscriptcluster.db annotation

updated 7.7 years ago by James W. MacDonald 67k • written 7.7 years ago by Khawaja • 0

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nsfilter affymetrix hugene10sttranscriptcluster.db annotation

updated 7.8 years ago by James W. MacDonald 67k • written 7.8 years ago by hallie.cla • 0

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hugene10sttranscriptcluster.db annotation

updated 9.5 years ago by James W. MacDonald 67k • written 9.5 years ago by colonppg ▴ 30

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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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