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SVAseq
•
reset
0
votes
1
reply
638
views
how to identify the unwanted variables independent of phenotypes
RUVSeq
svaseq
22 months ago
Tongjun
• 0
0
votes
0
replies
1.1k
views
SVA method for estimating surrogate variables of RNA Seq
RNASeq
sva
svaseq
updated 2.3 years ago by
James W. MacDonald
65k • written 2.3 years ago by
Bex
• 0
0
votes
0
replies
790
views
SVAseq for differential transcript usage and differential splicing analysis
limma
sva
Leafcutter
SVAseq
2.6 years ago
georgia.katsoula
▴ 40
0
votes
1
reply
768
views
SVA for visualisation purposes
sva
svaseq
surrogate variable analysis
updated 4.1 years ago by
James W. MacDonald
65k • written 4.1 years ago by
Mozart
▴ 30
1
vote
1
reply
925
views
svaseq - over adjustment
svaseq
sva
5.1 years ago
flippy23
• 0
1
vote
1
reply
879
views
sva correction for MEDIPS
MEDIPS
svaseq
sva
updated 5.3 years ago by
Lukas Chavez
▴ 570 • written 5.3 years ago by
tofukaj
• 0
2
votes
3
replies
1.5k
views
Batch-effect: batch in design and corrected batch with sva- DESeq2
deseq2
svaseq
5.3 years ago
bioinfo
• 0
3
votes
4
replies
1.5k
views
Calling svaseq() multiple times
edger
sva
svaseq
limma
updated 6.0 years ago by
Ryan C. Thompson
★ 7.9k • written 6.0 years ago by
cats_dogs
▴ 20
1
vote
2
replies
3.1k
views
Applying SVA to RNA-Seq dataset
DESeq2
sva
svaseq
batch effect correction
6.3 years ago
L_K
• 0
0
votes
0
replies
1.1k
views
correlated known batch effect correction using svaseq
svaseq
batcheffectcorrection
6.5 years ago
burcu.atasu
• 0
1
vote
1
reply
1.5k
views
Outputting batch-effect free normalized counts
ruvseq
svaseq
edaseq
updated 6.5 years ago by
davide risso
▴ 950 • written 6.5 years ago by
llo
▴ 10
0
votes
0
replies
1.2k
views
Batch correction with uncertain biological variables
sva
svaseq
batch effect
batch effects
batch effect correction
6.7 years ago
vedran.franke
• 0
1
vote
6
replies
1.7k
views
RNASeq fold change analysis after subtraction of contaminating MEF signal
deseq2
svaseq
updated 6.7 years ago by
Michael Love
42k • written 6.7 years ago by
gpalidwor
▴ 10
3
votes
4
replies
1.7k
views
Taking surrogate variable into account before running PCA
sva
svaseq
updated 6.9 years ago by
Guido Hooiveld
★ 3.9k • written 6.9 years ago by
wamiqsaifi
• 0
3
votes
2
replies
2.5k
views
(batch) corrections of RNA-seq data: integrating LIMMA and SVA
limma
sva
svaseq
updated 7.2 years ago by
Aaron Lun
★ 28k • written 7.2 years ago by
Bogdan
▴ 670
2
votes
7
replies
1.8k
views
Is possible to apply 'svaseq' with 'DEXSeq' design in order to remove unknown batch effects ?
svaseq
dexseq
updated 7.2 years ago by
Alejandro Reyes
★ 1.9k • written 7.3 years ago by
tofukaj
• 0
3
votes
6
replies
2.3k
views
is it necessary to check batch effect in this case? and how to?
svaseq
combat sva
RANseq
batcheffect
removebatcheffect
updated 7.5 years ago by
Jakub
▴ 50 • written 7.5 years ago by
amoltej
▴ 10
5
votes
7
replies
5.2k
views
Correcting for known and surrogate variables in DESeq2
deseq2
svaseq
7.6 years ago
Akula, Nirmala NIH/NIMH [C]
▴ 190
2
votes
1
reply
1.7k
views
Regarding batch effect in Deseq2 package
deseq2
sva
svaseq
updated 7.7 years ago by
Michael Love
42k • written 7.7 years ago by
szenitha
▴ 20
0
votes
3
replies
2.4k
views
can we use sva function to estimate artifacts for rna seq data?
sva
svaseq
batcheffectcorrection
updated 7.7 years ago by
Jeff Leek
▴ 650 • written 7.7 years ago by
szenitha
▴ 20
1
vote
5
replies
3.7k
views
PCA of svaseq "cleaned" counts and DESeq2 SV subtracted counts are different?
deseq2
sva
svaseq
pca
7.9 years ago
Peter Alto
▴ 10
21 results • Page
1 of 1
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Comment: Mac ARM64 build report for BioC 3.19 from 'kjohnson3' reporting ERROR which it
by
Hervé Pagès
16k
Indeed. Calculations involving floating point arithmetic are architecture-dependent, and testing the results should be done with `all.equal…
Comment: How to use bootRanges to bootstrap small RNA loci (nullranges package)
by
Poonam
• 0
I will follow what you suggested. I didn't use max gap anywhere. I was following statistic I and regarding the size of features, my small…
Comment: How to use bootRanges to bootstrap small RNA loci (nullranges package)
by
Michael Love
42k
Oh I see, for the second question, I don't have a great answer. I typically think of one set as the anchor, whose ascertainment is driving …
Comment: Help with running egsea()
by
James W. MacDonald
65k
Oh, right. Ideally you would use NCBI (aka Entrez gene) IDs because they are way more likely to be unique. Gene symbols are broken down int…
Comment: Help with running egsea()
by
Chris
• 0
Thanks James! I update the question. The last question mean when we use `buildIdx()`, could we use gene symbol instead of entrezID. However…
Votes
Answer: How to save the DEXSeq results
Answer: minfi support of illumina Infinium methylationEPIC v2.0
Comment: minfi support of illumina Infinium methylationEPIC v2.0
Answer: Mac ARM64 build report for BioC 3.19 from 'kjohnson3' reporting ERROR which it
Comment: Help with running egsea()
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