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rnaseqrdata
•
reset
1
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4
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812
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RNA-seq analysis between a wildtype vs a double microRNA kockout mouse brain
microRNA
gene
RNASeqRData
edgeR
geneontology
18 months ago
faiza
• 0
1
vote
3
replies
675
views
What should I do with RNA-Seq data to get a gene that work?
find
RNASeqRData
updated 18 months ago by
ATpoint
★ 4.1k • written 18 months ago by
yuhang
• 0
1
vote
4
replies
1.4k
views
merge TPM values for same geneID
RNASeqRData
TPM
updated 19 months ago by
ATpoint
★ 4.1k • written 19 months ago by
prashali.bansal
▴ 10
0
votes
0
replies
471
views
how to create PHENO_DATA
RNASeq
RNASeqData
RNASeqRData
20 months ago
marymshahi2021
• 0
0
votes
1
reply
600
views
DeSeq2 timecourse analysis
RNAseqRData
DeSeq2
updated 2.1 years ago by
Michael Love
41k • written 2.1 years ago by
Hannah
• 0
0
votes
17
replies
3.2k
views
results(dds) error: couldn't find results. you should first run DESeq()
RNASeqRData
updated 2.2 years ago by
Michael Love
41k • written 2.2 years ago by
beslinail
• 0
1
vote
1
reply
788
views
edgeR for SDE analysis
RNASeqRData
edgeR
RNASeqR
RNASeqData
updated 2.2 years ago by
Gordon Smyth
50k • written 2.2 years ago by
vikycairoli
• 0
1
vote
2
replies
884
views
Is 100K genes too many to run ComBat_seq on?
RNASeqRData
combat_Seq
BatchEffect
2.6 years ago • updated 2.3 years ago
zeegzaag
• 0
0
votes
1
reply
866
views
Limma Voom Design and Contrast Matrix- Can my parameter also be a factor?
RNASeqRData
limma
RNASeq
RNASeqR
updated 3.1 years ago by
Gordon Smyth
50k • written 3.1 years ago by
Rita
• 0
2
votes
2
replies
2.7k
views
How to download KEGG pathways for list of enriched genes
RNASeqRData
GO
3.2 years ago
Wuschel
▴ 10
0
votes
0
replies
737
views
display .CT files in a BioC package
RNAinteract
rnaseqGene
RNASeqRData
rnaseqcomp
3.2 years ago
Bogdan
▴ 670
4
votes
4
replies
1.1k
views
DEseq2: working with unbalanced number of sample in tumor study?
Deseq2
RNASeqRData
unbalancedsamplesize
updated 23 months ago by
Michael Love
41k • written 3.2 years ago by
Cihat
• 0
1
vote
5
replies
2.1k
views
How can I use bioconductor and Deseq2 in linux ubuntu 18
RiboProfiling
DESeq2
Bioconductor
RNASeqRData
updated 18 months ago by
Kevin Blighe
★ 3.9k • written 3.3 years ago by
Taufiq
• 0
13 results • Page
1 of 1
Recent ...
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Comment: How to use bootRanges to bootstrap small RNA loci (nullranges package)
by
Poonam
• 0
I looked into the genomic distributions. Please see the screenshot attatched ![ distrubution for female loci, boot1 and boot2][1] how do …
Answer: How to save the DEXSeq results
by
Michael Love
41k
If you look at the output here: https://bioconductor.org/packages/release/bioc/vignettes/DEXSeq/inst/doc/DEXSeq.html#4_Testing_for_differe…
Answer: Method to find pathways different between 2 groups
by
Robert Castelo
★ 3.3k
Hi, regarding how could you combine the result from each tool, one option is using a so-called "ensembl method", for instance, the package …
Answer: Couldn't connect to server while using "pathways"
by
James W. MacDonald
65k
As ATpoint already noted, you should proceed from the assumption that your audience knows nothing about what you are doing, and provide eno…
Answer: Trim/Filter out-of-bounds GRanges
by
Michael Love
41k
https://support.bioconductor.org/p/73432/#73448
Votes
Answer: Method to find pathways different between 2 groups
Answer: Method to find pathways different between 2 groups
Answer: Why does GSEA on edgeR results for randomized samples give highly significant p-
Answer: Method to find pathways different between 2 groups
Comment: Trying to use enrichGO
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