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HTSeqCounts
•
reset
0
votes
4
replies
1.8k
views
Normalise counts when tumour samples have normal tissue contamination.
deseq2
deseq
edgeR
rnaseq
htseqcounts
7.9 years ago
Deepali
• 0
0
votes
3
replies
2.5k
views
how to read htseq-count
edger
htseqcounts
updated 8.0 years ago by
Gordon Smyth
53k • written 8.0 years ago by
Bioinformatics
▴ 30
1
vote
1
reply
2.8k
views
Difference between SummarizeOverlaps and HTSeq
R
summarizeoverlaps
htseqcounts
updated 8.2 years ago by
thokall
▴ 160 • written 8.2 years ago by
Walter F. Baumann
▴ 10
1
vote
2
replies
5.2k
views
Length of 'group' must equal number of columns in 'counts'
htseqcounts
edger
updated 3.3 years ago by
Randy
• 0 • written 8.4 years ago by
mictadlo
▴ 10
3
votes
7
replies
4.0k
views
read counts for each gene for edgeR
edger
htseqcounts
updated 8.4 years ago by
Gordon Smyth
53k • written 8.4 years ago by
mictadlo
▴ 10
2
votes
2
replies
1.6k
views
Why does total unique map not equal to library size?
htseqcounts
star
rnaseq
8.4 years ago
Ahdee
▴ 60
0
votes
5
replies
3.0k
views
FeatureCounts output to SAM like htseq-counts?
featurecounts
SAM
htseqcounts
updated 2.5 years ago by
Yang Liao
▴ 450 • written 8.7 years ago by
courtney.stairs
• 0
2
votes
4
replies
4.2k
views
Error in DESeqDataSetFromHTSeqCount: Gene IDs (first column) differ between files.
chipseq
deseq2
htseqcounts
updated 2.9 years ago by
mhashan.j
▴ 10 • written 8.9 years ago by
JunLVI
▴ 40
1
vote
1
reply
1.4k
views
RNA-seq: EdgeR's togtags table not correlating to htseq-count's CPM values
edger
htseqcounts
rnaseq
updated 9.1 years ago by
Aaron Lun
★ 29k • written 9.1 years ago by
romsdahl
• 0
0
votes
0
replies
1.4k
views
DEXSeq error: erro in dexseq_count.py
dexseq_count
dexseq
htseqcounts
9.3 years ago
as1023
• 0
0
votes
7
replies
2.3k
views
PCA results different from th same sample but different counting method
deseq2
pca
tximportdata
htseqcounts
updated 9.5 years ago by
Michael Love
43k • written 9.5 years ago by
jarod_v6@libero.it
▴ 40
1
vote
4
replies
2.3k
views
GOSeq: analysis of unsupported genome after HTseq and DEseq2 - building gene lengths, comparing contrasts and understanding results.
deseq2
goseq
htseqcounts
rnaseq
plant
updated 9.6 years ago by
Gordon Smyth
53k • written 9.6 years ago by
Ben Mansfeld
• 0
1
vote
6
replies
2.6k
views
Error: could not find function "HTSeqCounts"
HTSeq
HTSeqCounts
Could not find function
DEXSeq
updated 9.7 years ago by
Martin Morgan
25k • written 9.7 years ago by
sakura.nussbaum
▴ 10
13 results • Page
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Comment: DESeq2 - how many surrogate variables from svaseq, use of lfcshrink
by
ja569116
• 0
Hi @atpoint Thanks for the information. Could you please expand on when to use adjusted p-values vs nominal p-values. My understanding was …
Answer: limpa analysis advice
by
Gordon Smyth
53k
It is actually very hard to estimate the DPC from observed data, because the curve is function of unobserved intensities rather than a func…
Answer: When to use edgeR or limma
by
Gordon Smyth
53k
The short answer is that we generally prefer edgeR for applications with lots of small counts and limma for complex designs with random eff…
Comment: limpa-blank normalization and Spectronaut's PTM stoichiometry
by
Gordon Smyth
53k
I updated the above answer today.
Answer: When to use edgeR or limma
by
James W. MacDonald
68k
I would use edgeR's quasi-likelihood model for any analysis with a smaller number of observations (like 3 vs 3 or similar), but if you have…
Votes
Answer: When to use edgeR or limma
Answer: When to use edgeR or limma
Answer: When to use edgeR or limma
Answer: When to use edgeR or limma
A: deseq2 - paired samples in 2 sequencing types with very different library sizes
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