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graper 1.22 Build is Broken
bug
graper
offtopic
updated 8 weeks ago by
shepherl
4.1k • written 8 weeks ago by
Bjarne
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Spam:
Small Business Directory Emerald Coast
BUScorrect
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updated 4 months ago by
shepherl
4.1k • written 4 months ago by
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Why is RNA-Seq library size not constant among samples?
RNA-Seq
sequencer
library_size
sequency_depth
multiplexing
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updated 24 months ago by
James W. MacDonald
68k • written 24 months ago by
FedeXandeR
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Genomics data
mygene
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updated 2.2 years ago by
James W. MacDonald
68k • written 2.2 years ago by
Shila
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ERROR IN INSTALLATION PACKAGE IN R
derfinderData
SpikeInSubset
musicatk
Guitar
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updated 2.5 years ago by
Marcel Ramos
700 • written 2.5 years ago by
Chanchal
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1.9k
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Extract specific portion of a string and paste to a new column in R
Rscript
tidyr
dataframe
tidyverse
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updated 2.7 years ago by
Marcel Ramos
700 • written 2.7 years ago by
Nikhil
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Editing Plots Generated Using MicrobiomeAnalyst
MicrobiomeData
microbiome
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updated 3.8 years ago by
James W. MacDonald
68k • written 3.8 years ago by
gwagz8
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DiffBind Normalisation between Narrow/Broad Peaks from different peak callers
ChIPSeq
SICER2
DiffBind
MACS2
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updated 3.9 years ago by
James W. MacDonald
68k • written 3.9 years ago by
Yuan Tian
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Comment: Cannot extract size factor from DESeq2 analysis
by
s.malik
• 0
Dear Mike, using tximeta and following code, is this fine to extract normalized counts after `sizeFactors(dds)` gives NULL? `dds <- DESeq…
Comment: Design formula for circadian time-course data for vst() function
by
Vishnu
• 0
Thank you so much for your reply.
Comment: Analyzing TnSeq data with DESeq2
by
Tom
• 0
[Doncaster Locksmith][1] delivers trusted, efficient security services tailored to your needs. Analyzing TnSeq data with DESeq2 may uncover…
Answer: Design formula for circadian time-course data for vst() function
by
ATpoint
★ 4.8k
This was asked before: https://support.bioconductor.org/p/9148734/#9148812 Take-home message is that influence is minor, as you see your…
Comment: Filtering after DESeq
by
caroline.zanchi
• 0
... I did it. It does filter out quite a bit of genes : ``` keep <- filterByExpr(dds, group="host_treatment_generation",min.count = 10, mi…
Votes
A: DESeq2::sizeFactors() function does not output the sizeFactor table.
Comment: Filtering after DESeq
A: Normalized counts from DESeq2 results in similar but not equal total read count?
A: DESeq2: Different Dispersions for different sample groups
A: Contrasts & coefficients in limma
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