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Retrieving Package Metadata from Bioconductor API: Versions and Dependencies
metaMSdata
updated 4 months ago by 4.1k • written 4 months ago by • 0
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Spam: How do professional SEO services enhance user experience on my website?
metaMSdata
5 months ago Steven 0
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How to search Pubmed Central or other fulltext literature base using regex?
metaMSdata Bioconductor
5 months ago Abiologist • 0
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News: Stop mirror service
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updated 6 months ago by 4.1k • written 6 months ago by • 0
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Can log2cpm be used for proteomics data normalization?
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7 months ago Daniel • 0
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featureCounts reports an error:"featureCounts: input-files.c:2890: SAM_pairer_get_next_read_BIN: Assertion `l_name < 256' failed. Aborted (core dumpe…
metaMSdata
7 months ago shuwangxinze1996 • 0
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Doing comparison of RNA-seq data using EdgeR
metaMSdata edgeR
updated 8 months ago by 52k • written 8 months ago by • 0
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Visium RNA
metaMSdata
written 9 months ago by • 0
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How to control RAN-seq samples from different libraries
metaMSdata
updated 10 months ago by 67k • written 10 months ago by • 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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