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DEseq
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208
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Volcano plot becomes flipped when I add a third condition
DESeq2
volcanoplot
deseq
HELP
contrast
updated 27 days ago by
Basti
▴ 700 • written 4 weeks ago by
Michael
• 0
0
votes
1
reply
165
views
What is the difference between these two arguments for log fold change shrinkage?
DESeq
updated 7 weeks ago by
Michael Love
39k • written 7 weeks ago by
m-bihie
▴ 10
0
votes
1
reply
165
views
Is it possible to convert transcript-level to gene-level dataset to use it in DESeq2 ?
DESeq2
Transcriptomics
tximport
deseq
txi
updated 8 weeks ago by
Dario Strbenac
★ 1.5k • written 9 weeks ago by
Hicham
• 0
0
votes
2
replies
815
views
suggestions/comments on DESeq transcript wise analysis
convert
DESeq
convert
DESeq
written 11.1 years ago by
Akula, Nirmala NIH/NIMH [C]
▴ 190
1
vote
1
reply
211
views
How to design multifactor DESEQ2 formula?
DESEQ
DESEQ2
updated 6 months ago by
ATpoint
★ 2.3k • written 6 months ago by
barrypraveen
• 0
3
votes
2
replies
349
views
DESeq2 is renaming gene names and lack of downregulated genes
DESeq
DESeq2
7 months ago
manwar
• 0
1
vote
1
reply
321
views
Gene wise dispersion estimate Process - From the prior to the posterior
GLM
prior
DESeq
LFC
updated 9 months ago by
Michael Love
39k • written 9 months ago by
stew
• 0
1
vote
5
replies
482
views
Error in DEseq
DEseq
RNASeqData
updated 9 months ago by
ATpoint
★ 2.3k • written 9 months ago by
Sanatan
• 0
2
votes
1
reply
550
views
Difference between raw counts and featureCounts for DESeq2
deseq
featurecounts
counts
DESeq2
updated 10 months ago by
swbarnes2
★ 1.2k • written 10 months ago by
Hicham
• 0
1
vote
5
replies
665
views
Potential outlier/high variance
deseq
DESeq2
updated 10 months ago by
Michael Love
39k • written 11 months ago by
Amali Thrimawithana
• 0
0
votes
1
reply
2.3k
views
voom() vs. RPKM/FPKM or otherwise normalized counts, and GC correction, when fitting models to a small number of responses (per-feature counts)
Normalization
graph
limma
convert
edgeR
DESeq
Rsubread
Normalization
graph
limma
convert
updated 11 weeks ago by
Gordon Smyth
47k • written 10.8 years ago by
Kasper Daniel Hansen
6.5k
11 results • Page
1 of 1
Recent ...
Replies
Comment: Does DiffBind make consensus peaks sets for samples from a given condition (e.g.
by
tahir.msajid
• 0
Hi Rory, I came up with another question while analyzing my data. A scenario of analysis: Path to bam files, path to peaks files (broad pe…
Comment: How to deal with the negative values from EBPlusPlusAdjustPANCAN_IlluminaHiSeq_R
by
Yang Shi
▴ 10
Thanks for your reply sir! Here is the data ([EBPlusPlusAdjustPANCAN_IlluminaHiSeq_RNASeqV2.geneExp.tsv][1]). And there is the data process…
Comment: TxDB.Hsapiens.UCSC.hg38.knownGene with locateVariants() identifying SNPs from va
by
davidhillis
• 0
Thank you!
Comment: Time-course, comparison of two groups
by
boczniak767
▴ 720
Thank you Gordon for your time and patience, I'd try to be more specific. I've read carefully the three first chapters of `edgeR` user guid…
Comment: TxDB.Hsapiens.UCSC.hg38.knownGene with locateVariants() identifying SNPs from va
by
James W. MacDonald
62k
This works for me. ``` > library(VariantAnnotation) > library(TxDb.Hsapiens.UCSC.hg19.knownGene) > txdb <- TxDb.Hsapiens.UCSC.hg19.knownGe…
Votes
Comment: TxDB.Hsapiens.UCSC.hg38.knownGene with locateVariants() identifying SNPs from va
A: Pathway analysis of differentially methylated CpGs
Comment: TxDB.Hsapiens.UCSC.hg38.knownGene with locateVariants() identifying SNPs from va
Comment: TxDB.Hsapiens.UCSC.hg38.knownGene with locateVariants() identifying SNPs from va
Answer: TxDB.Hsapiens.UCSC.hg38.knownGene with locateVariants() identifying SNPs from va
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