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epicv2
•
reset
1
vote
2
replies
1.2k
views
CpGs with genomic positions greater than the chromosome size in EPICv2?
EPICv2
EPICv2manifest
5 weeks ago • updated 4 weeks ago
Joshua Llano
• 0
2
votes
7
replies
3.1k
views
Annotation for EPICv2
EpicV2
ChAMPdata
updated 5 months ago by
icecreamlover
• 0 • written 6 months ago by
nurkenber
• 0
1
vote
9
replies
3.5k
views
Error using champ.import
ChAMP
EPICv2
updated 6 months ago by
Ricky
• 0 • written 22 months ago by
medha.suman
• 0
0
votes
0
replies
311
views
DMRcate pcutoff setting
EpicV2
DMRcate
6 months ago
kitzhu
• 0
1
vote
3
replies
1.6k
views
SeSAMe DMR for EPIC V2
sesame
EPICv2manifest
epicv2
10 months ago
luca.s
▴ 50
0
votes
2
replies
1.1k
views
Combining analysis of EPICv1 and EPICv2 using SeSAMe package
sesameData
EPICv2
EPICv1
updated 6 months ago by
zhouwanding
▴ 20 • written 10 months ago by
archibold.mposhi
• 0
3
votes
2
replies
925
views
limma Intercept vs No-intercept models completely changing DMR results?
limma
DMRcate
MethylationArray
EPICV2
updated 11 months ago by
Gordon Smyth
52k • written 12 months ago by
Kim
• 0
1
vote
3
replies
1.9k
views
Error in GOmeth function of missMethyl when EPICv2 annotation is used
DNAMethylation
GO
MethylationArray
missMethyl
EPICv2
14 months ago • updated 7 months ago
s.malik
• 0
0
votes
4
replies
2.0k
views
Seeking Strategies for Managing Duplicate CpG Entries in EPIC v2 Manifest
DNAMethylation
EPICv2
IlluminaHumanMethylationEPICmanifest
updated 14 months ago by
James W. MacDonald
68k • written 14 months ago by
rae.alshammari
▴ 20
0
votes
4
replies
3.0k
views
ChAMP - obtaining beta values using EPICv2 annotation
ChAMP
EPICv2
updated 5 months ago by
icecreamlover
• 0 • written 15 months ago by
ChunkyJones
• 0
3
votes
5
replies
1.9k
views
Looking for equivalent EPIC chip v1 vs. v2 annotation variables
sesame
IlluminaHumanMethylationEPICv2anno.20a1.hg38
methylationEPICv2.0
EpicV2
updated 13 months ago by
aldea85
• 0 • written 17 months ago by
Courtney
▴ 10
1
vote
6
replies
3.0k
views
annotation EpicV2
minfiDataEPIC
EpicV2
updated 19 months ago by
Zuguang Gu
▴ 290 • written 20 months ago by
Izabela.ams
▴ 10
12 results • Page
1 of 1
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Replies
Comment: How can I correctly use phyloseq with Docker?
by
James W. MacDonald
68k
You can use [bioc-run][1] to simplify things as well. [1]: https://github.com/Bioconductor/bioc-run/tree/devel
Comment: How can I correctly use phyloseq with Docker?
by
James W. MacDonald
68k
You show how you modified the container, but not how you are running it, which is the critical part.
Comment: Discrepancies in normalised count data vs unnormalised
by
AMgroup
• 0
Thank you for your reply. > Per sample all counts are scaled by the same size factor so I strongly assume that something was parsed here …
Comment: Discrepancies in normalised count data vs unnormalised
by
ATpoint
★ 4.8k
Please show examples using `plotCounts()`. Custom spreadsheets harbor the risk of parsing errors along the way which very often explains wh…
Comment: Cannot extract size factor from DESeq2 analysis
by
s.malik
• 0
Dear Mike, using tximeta and following code, is this fine to extract normalized counts after `sizeFactors(dds)` gives NULL? `dds <- DESeq…
Votes
Answer: How to combine two DESeq2 objects (dds) for analysis
How to combine two DESeq2 objects (dds) for analysis
How can I correctly use phyloseq with Docker?
A: DESeq2::sizeFactors() function does not output the sizeFactor table.
Comment: Filtering after DESeq
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