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SpikeIn
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0
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440
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Spike-in normalization method in ATACseq
sperm
Drosophila_melanogaster
ATACSeq
Normalization
SpikeIn
updated 3 months ago by
ATpoint
★ 4.6k • written 3 months ago by
Katerina
• 0
0
votes
2
replies
401
views
Analysis of transcription inhibition with DESeq2
SpikeIn
DESeq2
Normalization
written 5 months ago by
ADopico
• 0
0
votes
1
reply
575
views
Problem with spike-ins (ERCC) in DESeq2 analysis after doing RUVg!
SpikeIn
RUVSeq
DESeq2
RUV
updated 6 months ago by
Michael Love
43k • written 7 months ago by
Ειρήνη
• 0
0
votes
0
replies
323
views
Diffbind Error in socketConnection
DiffBind
Errorinsocketconnection
SpikeIn
9 months ago
Virangika
• 0
1
vote
2
replies
817
views
DiffBind spike-in lib.sizes confusion
SpikeIn
DiffBind
23 months ago
Weisheng
• 0
6
votes
2
replies
3.2k
views
Clarification of what DESeq2::estimateSizeFactors controlGenes does and when it should *not* be used
DESeq2
SpikeIn
Normalization
DifferentialExpression
updated 2.0 years ago by
ATpoint
★ 4.6k • written 2.0 years ago by
kalavattam
▴ 10
0
votes
2
replies
2.3k
views
How to use spike-in information (sequences from another species) with DESeq2::DESeq()
DESeq2
SpikeIn
Normalization
updated 8 months ago by
maria.soler
• 0 • written 2.0 years ago by
kalavattam
▴ 10
3
votes
4
replies
2.4k
views
RiP RLE normalisation using spike-in peaks in DiffBind for ChIP-seq
DiffBind
SpikeIn
Normalization
ChIP-seq
csaw
2.1 years ago
spg
• 0
0
votes
0
replies
1.1k
views
DiffBind spike-in normalisation with varying amounts of spike-in chromatin
DiffBind
ChIPSeq
Normalization
SpikeIn
3.3 years ago
Drew
• 0
0
votes
0
replies
922
views
Spike-In Cells for Normalization?
SpikeIn
SingleCell
3.4 years ago
mb1996
• 0
0
votes
2
replies
1.5k
views
Using both spike in and TMM normalizations in ChIP-seq samples
ChIPSeq
SpikeIn
edgeR
Normalization
3.5 years ago
maria.soler
• 0
7
votes
12
replies
4.9k
views
Using edgeR and a spike-in to calculate absolute abundance
edgeR
SpikeIn
RNASeq
updated 16 months ago by
Miguel
• 0 • written 3.9 years ago by
robert.chen
• 0
1
vote
9
replies
3.9k
views
Spike-in normalization in EdgeR
CUTandRUN
edgeR
Normalization
SpikeIn
ChIPSeq
updated 2.2 years ago by
Bogdan
▴ 670 • written 4.3 years ago by
Hesh
▴ 10
13 results • Page
1 of 1
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Comment: displaying the differential expression with deseq2 over 4X2 samples with the in
by
Martijn
• 0
thanks James, but if I do pairwise analyses per subject, I get the impression that I only get the intercepts per gene. Do you mean regardin…
Comment: plyranges: find exact GRanges match keeping metadata columns
by
alexis.weinreb
• 0
Thank you, this does clarify the available options.
Answer: displaying the differential expression with deseq2 over 4X2 samples with the in
by
James W. MacDonald
67k
If you have paired data you should block on subject, which is algebraically the same as fitting a model on the difference between treated a…
Answer: How to compare expression levels of genes between scRNAseq and bulkRNAseq?
by
jodan
• 0
Your approach sounds solid! You might also consider plotting a scatter plot comparing log2 fold changes from both datasets to identify gene…
Answer: Unused arguments error without used arguments in GSVA?
by
jodan
• 0
It looks like the ssgseaParam function might not be passing the correct parameters to GSVA::gsva(). The error suggests that minSize and max…
Votes
Answer: Find exact GRanges match keeping metadata columns
Answer: Find exact GRanges match keeping metadata columns
Answer: Unused arguments error without used arguments in GSVA?
Answer: Unused arguments error without used arguments in GSVA?
Answer: Unused arguments error without used arguments in GSVA?
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