8.2 years ago • updated 8.1 years ago
philipp24
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8.1 years ago
philipp24
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updated 5.6 years ago by
James W. MacDonald
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written 5.6 years ago by
moldach
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written 7.8 years ago by
graggsd
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updated 2.8 years ago by
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yoursbassanio
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updated 7.1 years ago by
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written 7.1 years ago by
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updated 7.2 years ago by
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8.1 years ago
philipp24
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belinda.phipson
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6.0 years ago
Taub, Margaret
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5.9 years ago
owen.whitley
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updated 2.8 years ago by
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written 3.7 years ago by
stewart999
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updated 12 months ago by
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updated 9 weeks ago by
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Comment: Extremely small p-values using Limma for proteomic data
by
James W. MacDonald
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If you ever find yourself using the `@` function, you should reconsider what you are doing. There are vanishingly small instances when an e…
Comment: How to use bootRanges to bootstrap small RNA loci (nullranges package)
by
Michael Love
42k
Here is some example code
<https://gist.github.com/mikelove/cbbc84634b6854c865cb5eb08ad9b245>
Comment: How to use spike-in information (sequences from another species) with DESeq2::DE
by
maria.soler
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0
Hi, I have a question barely related to this topic. Do you use a custom reference genome combining your organism and the one used as a spik…
Answer: Differential gene expression analysis results
by
ATpoint
★
4.1k
Pease do not open multiple posts for the same issue: https://support.bioconductor.org/p/9158194/#9158222
The support site is not meant f…
Comment: deseq2 results
by
sajadahmad41454
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0
thank you for your response, should i remove or discard that sample? since the red outlier on left represents one of healthy samples.
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