Bioconductor Reads

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1.2k

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DiffBind Reads MACS2 FullLibSize

updated 13 months ago by Rory Stark ★ 5.2k • written 13 months ago by Marianna ▴ 20

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2.1k

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boxplot reads fastq sequencing rsubread

updated 6.2 years ago by Wei Shi ★ 3.6k • written 6.3 years ago by Raito92 ▴ 60

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1.3k

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rna-seq reads

updated 6.3 years ago by Gordon Smyth 52k • written 6.3 years ago by Ramiro Magno ▴ 100

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1.5k

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dexseq reads

8.2 years ago 514028929 • 0

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1.3k

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diffbind reads bamfiles

updated 8.4 years ago by Rory Stark ★ 5.2k • written 8.4 years ago by kbrnrc • 0

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2.2k

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genomicranges reads genomicfeatures Bam

10.5 years ago gen ▴ 30

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3.6k

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deseq filter reads

10.6 years ago ccheung • 0

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2.7k

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reads

updated 10.9 years ago by James W. MacDonald 68k • written 10.9 years ago by marcovth • 0

8 results • Page 1 of 1

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Comment: WGCNA analysis on RNAseq and proteoimcs data by sum31278 • 0

Hi sagigordon, Can you share how you performed WGCNA analysis for proteomics data? Thanks

Comment: European Bioconductor Conference 2023 planning by inadequate.peacock.iiag • 0

I once faced a dilemma similar to this when coordinating a smaller local event; despite initial hesitation, I learned invaluable skills and…

Comment: ROAST compare results with complex design by Gordon Smyth 52k

It's also worth pointing out that the syntax for `camera` and `mroast` is the same, so I wonder how OP did the earlier `camera` analysis.

Answer: ROAST compare results with complex design by James W. MacDonald 68k

You are specifying that the last column of your design should be used as the contrast. You should instead use `contrast[,1]`, which will us…

Comment: How to account for solvent controls in DESeq2 when comparing follicular vs lutea by James W. MacDonald 68k

Yes. You can infer that by figuring out what each coefficient measures. Here is your design matrix: ``` > targets ID Name phase G…

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Answer: ROAST compare results with complex design

How to account for solvent controls in DESeq2 when comparing follicular vs luteal phase?

Answer: How to account for solvent controls in DESeq2 when comparing follicular vs lutea

Comment: Using DESeq2 on single cell RNA Seq data of same cell type but different conditi

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