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HI-C
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diffHic ICE normalization PCA with NAs
diffHic
normalization
pca
NAs
HI-C
updated 6.0 years ago by
Aaron Lun
★ 28k • written 6.0 years ago by
inzirio
▴ 10
1
vote
5
replies
2.1k
views
visualize Hi-C .cool file in R
Hi-C
HiTC
6.8 years ago
ta_awwad
▴ 10
3
votes
2
replies
2.9k
views
Best way to get HiCUP-mapped Hi-C data into diffHiC
hicup
hi-c
diffhic
homer
7.8 years ago
e.jacobson
▴ 10
1
vote
4
replies
2.2k
views
Is there a way to align Hi-C half heatmaps to Gviz track?
Gviz
Hi-C
Heatmap
updated 9.0 years ago by
Nicolas Servant
▴ 260 • written 9.0 years ago by
Merienne Nicolas
▴ 120
1
vote
10
replies
2.7k
views
FourC object from scratch
hi-c
HiTC
fourcseq
9.5 years ago • updated 9.4 years ago
Nicolas Servant
▴ 260
2
votes
4
replies
2.0k
views
diffHic-package_PreparePairs-function-error:"missing chromosomes in cut site list"
diffHic
PreparePairs
Hi-c
cutGenome
9.9 years ago • updated 9.8 years ago
rulicosentino
• 0
6 results • Page
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Comment: CluserProfiler message "No gene can be mapped"
by
Carolina
• 0
There is, the overlap that reads out is ( Genes in common: 368 of 368 ). Here is the link for [background genes][1], [term2gene][2], [term2…
Comment: Differing results with DESeq2
by
JKim
• 0
My two cents. I think it would be more straightforward if you use cellmeans model. Have a look at [A guide to creating design matrices for …
Answer: CluserProfiler message "No gene can be mapped"
by
James W. MacDonald
68k
Your gene IDs are things like this: `Mpyr-NLJ1B.v3.hap1.scaffold1.g290550`, and the genes in your term2gene table are things like this: `Mp…
Answer: RNA-seq input to GRaNIE
by
James W. MacDonald
68k
This is [covered in the vignette.][1] [1]: https://bioconductor.org/packages/release/bioc/vignettes/GRaNIE/inst/doc/GRaNIE_packageDe…
Answer: Help using reduceSimMatrix with a custom annotation
by
sergisayolspuig
▴ 80
Hi there, `reduceSimMatrix()` expects a "GOALL" keytype in the OrgDb object when called with `children=TRUE` (which is the default for thi…
Votes
remove X and Y chromosome genes in RNA-seq data using DESeq2 pipeline
How to remove X & Y chromosome genes from RNAseq data
Is it advisable to remove X and Y chromosome genes in mouse bulk RNA-seq data at the level of the count matrix?
A: Unbalanced experiment with multiple samples from each patient.
A: Understanding contrasts limma
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