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HTSeqCounts
•
reset
0
votes
4
replies
928
views
Normalise counts when tumour samples have normal tissue contamination.
deseq2
deseq
edgeR
rnaseq
htseqcounts
5.1 years ago
Deepali
• 0
0
votes
3
replies
1.4k
views
how to read htseq-count
edger
htseqcounts
updated 5.2 years ago by
Gordon Smyth
47k • written 5.2 years ago by
Bioinformatics
▴ 30
1
vote
1
reply
1.4k
views
Difference between SummarizeOverlaps and HTSeq
R
summarizeoverlaps
htseqcounts
updated 5.4 years ago by
thokall
▴ 160 • written 5.4 years ago by
Walter F. Baumann
▴ 10
1
vote
2
replies
3.2k
views
Length of 'group' must equal number of columns in 'counts'
htseqcounts
edger
updated 5 months ago by
Randy
• 0 • written 5.5 years ago by
mictadlo
▴ 10
3
votes
7
replies
2.5k
views
read counts for each gene for edgeR
edger
htseqcounts
updated 5.5 years ago by
Gordon Smyth
47k • written 5.5 years ago by
mictadlo
▴ 10
2
votes
2
replies
892
views
Why does total unique map not equal to library size?
htseqcounts
star
rnaseq
5.5 years ago
Ahdee
▴ 50
0
votes
2
replies
1.5k
views
FeatureCounts output to SAM like htseq-counts?
featurecounts
SAM
htseqcounts
5.8 years ago
courtney.stairs
• 0
1
vote
4
replies
2.7k
views
Error in DESeqDataSetFromHTSeqCount: Gene IDs (first column) differ between files.
chipseq
deseq2
htseqcounts
updated 22 days ago by
mhashan.j
• 0 • written 6.1 years ago by
JunLVI
▴ 40
1
vote
1
reply
889
views
RNA-seq: EdgeR's togtags table not correlating to htseq-count's CPM values
edger
htseqcounts
rnaseq
updated 6.2 years ago by
Aaron Lun
★ 28k • written 6.2 years ago by
romsdahl
• 0
0
votes
0
replies
833
views
DEXSeq error: erro in dexseq_count.py
dexseq_count
dexseq
htseqcounts
6.5 years ago
as1023
• 0
0
votes
7
replies
1.3k
views
PCA results different from th same sample but different counting method
deseq2
pca
tximportdata
htseqcounts
updated 6.7 years ago by
Michael Love
39k • written 6.7 years ago by
jarod_v6@libero.it
▴ 40
1
vote
4
replies
1.3k
views
GOSeq: analysis of unsupported genome after HTseq and DEseq2 - building gene lengths, comparing contrasts and understanding results.
deseq2
goseq
htseqcounts
rnaseq
plant
updated 6.8 years ago by
Gordon Smyth
47k • written 6.8 years ago by
Ben Mansfeld
• 0
1
vote
6
replies
1.5k
views
Error: could not find function "HTSeqCounts"
HTSeq
HTSeqCounts
Could not find function
DEXSeq
updated 6.9 years ago by
Martin Morgan
25k • written 6.9 years ago by
sakura.nussbaum
▴ 10
13 results • Page
1 of 1
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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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