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Splicing
•
reset
0
votes
6
replies
1.6k
views
SGSeq error on analyzeFeatures
SGSeq
analyzeFeatures
Splicing
8.1 years ago
Paolo Guarnieri
▴ 20
1
vote
3
replies
1.4k
views
Microarray data analysis for detecting alternative splicing
microarray
splicing
updated 7.0 years ago by
Sonika Tyagi
▴ 20 • written 8.3 years ago by
gv
▴ 40
1
vote
2
replies
1.1k
views
Coverage function assigns wrong weights for gapped alignments
genomicalignments
splicing
coverage
updated 3.3 years ago by
Michael Lawrence
11k • written 5.8 years ago by
rasi1983
▴ 10
2
votes
2
replies
1.2k
views
Deseq2 alternative splicing in understudied organism
deseq2
splicing
updated 4.8 years ago by
Michael Love
39k • written 4.8 years ago by
yannickwurm
• 0
0
votes
1
reply
782
views
About CIRI's output
ciri
splicing
splicesites
updated 3.0 years ago by
lhddiallo
• 0 • written 4.7 years ago by
csijst
• 0
0
votes
1
reply
602
views
Can DEXseq be used for splicing QTL analysis?
dexseq
splicing
sqtl
qtl
updated 4.0 years ago by
Alejandro Reyes
★ 1.8k • written 4.0 years ago by
rtunney2
• 0
0
votes
1
reply
90
views
Transcriptome assembly: single individual or pooled samples
transcriptome
splicing
assembly
updated 11 weeks ago by
James W. MacDonald
62k • written 11 weeks ago by
Marianna
• 0
3
votes
16
replies
1.8k
views
Read counts generated by SGSeq are always 0
sgseq
splicing
alternative splicing
updated 6.9 years ago by
Leonard Goldstein
▴ 150 • written 6.9 years ago by
vakul.mohanty
▴ 10
1
vote
2
replies
1.1k
views
Is it possible to get Isoform-level differential isoform usage form DRIMSeq?
DRIMSeq
splicing
differential isoform usage
updated 6.0 years ago by
Gosia Nowicka
▴ 90 • written 6.0 years ago by
kristoffer.vittingseerup
▴ 20
2
votes
7
replies
1.3k
views
EdgeR diffSpliceDGE: Obtaining exon-level counts and normalisation step
edger
normalization
differential exon usage
splicing
updated 2.3 years ago by
Yunshun Chen
▴ 780 • written 2.3 years ago by
oakhamwolf
• 0
0
votes
3
replies
645
views
DEXSeq Splicing Result with incomplete lines between exons
DEXSeq
Splicing
Exon Usage
3.0 years ago
gunjan.dikshit
• 0
0
votes
0
replies
1.1k
views
DEXSeq analysis of alternative splicing: error 'SAM optional field tag NH not found'
DEXSeq
splicing
python
SAM
7.3 years ago
Fiona
▴ 70
0
votes
0
replies
367
views
Psichomics Suppa Input issue
psichomics
SUPPA
Splicing
Alternative Splicing
Retained Introns
2.3 years ago
noahhelton98
▴ 20
0
votes
1
reply
303
views
DEXSeq Exon count not working, please help with an alternative like featureCounts
splicing
Exon
featureCounts
subread
DEXSeq
8 months ago
NIK
• 0
0
votes
1
reply
489
views
JunctionSeq producing strangely large effect sizes for certain exon counting bins
junctionseq
splicing
RNAseq
DEXSeq
3.2 years ago
stuart
▴ 10
15 results • Page
1 of 1
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Comment: Which input file is used for DGEList in EgdeR?
by
mohammedtoufiq91
▴ 10
Thank you @gordonsmyth My collaborator asked me to test this pipeline with `egdeR` package. We are interested at gene level analysis only…
Answer: Why in Bioconductor community people rarely upvote questions?
by
Gordon Smyth
47k
I think it is a good idea to start a discussion with correct information. Looking back through Bioconductor Support records, it is not at a…
Comment: How to identify top most variable genes from log2 normalized data?
by
Gordon Smyth
47k
Your code doesn't look right to me. I think you're using order() where sort() would be more appropriate. To order your cpm matrix by row v…
Comment: How to load fasta file with openPrimeR?
by
Santiago Edilberto
• 0
> library(openPrimeR) There are missing/non-functioning external tools. To use the full potential of openPrimeR, please mak…
Answer: Which input file is used for DGEList in EgdeR?
by
Gordon Smyth
47k
I use and recommend featureCounts. Despite all that has been written on this topic, I still think that direct gene counting is faster and m…
Votes
Answer: Which input file is used for DGEList in EgdeR?
Answer: Identifying DEGs using lfcshrink()
Answer: Is this DESeq2 interactions design correct?
Comment: STRINGdb string_db$map error
Comment: How to normalize long-read RNA-seq data for comparison with short-reads
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