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ChIP-seq
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Job:
Bioinformatics position at the Department of Genetics, Stanford, California
next-generation sequencing
rna-seq
chip-seq
single cell
Job
9.5 years ago
Katja Hebestreit
▴ 130
0
votes
2
replies
2.3k
views
Diffbind plotting on contrasts
diffbind
chip-seq
updated 9.8 years ago by
AB
▴ 110 • written 10.8 years ago by
medinaale
• 0
0
votes
1
reply
3.0k
views
diffBind - bam not accessible
diffbind
chip-seq
bam
10.1 years ago
eli7javasky
• 0
3
votes
9
replies
3.9k
views
ChIPQC and broadPeak input
chipseq
chipqc
chip-seq
10.2 years ago
lindahove
▴ 10
0
votes
1
reply
1.7k
views
News:
Course Announcement: Use R / Bioconductor for Sequence Analysis (Intermediate Course)
Course
RNA-Seq
Chip-seq
Parallel
News
10.7 years ago
Martin Morgan
25k
4
votes
4
replies
2.1k
views
Strand-aware CSAW analysis
csaw
chip-seq
clip-seq
10.8 years ago
IV
▴ 30
2
votes
1
reply
1.6k
views
problem with characters in chromosome names in DiffBind dba
DiffBind
ChIP-Seq
updated 11.0 years ago by
Rory Stark
★ 5.2k • written 11.0 years ago by
Georg Otto
▴ 120
57 results • Page
2 of 2
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Comment: Getting a large intercept with DESeq2
by
Michael Love
43k
Thanks James -- Denise you can check the "note on factor levels" in the vignette. And I'd recommend `plotCounts()` for looking at individu…
Comment: Getting a large intercept with DESeq2
by
James W. MacDonald
68k
As a trivial example, consider this: ``` > model.matrix(~Treatment, data.frame(Treatment = factor(rep(1:3, each = 4)))) (Intercept) Tre…
Answer: Getting a large intercept with DESeq2
by
James W. MacDonald
68k
The default parameterization in R is a treatment-contrasts parameterization that sets one of your groups as the baseline. So the intercept …
Answer: Must I do pseudobulk analysis on Cell Surface Protein Labeling data of Single C
by
ATpoint
★ 5.0k
There is no "MUST", but pseudobulk aggregation is beneficial to a) enable use of tested and robust methods such as limma (though it could u…
Answer: Post translational modifications and phosphoproteomics in limpa?
by
Gordon Smyth
53k
Yes, we use limpa for PTMs ourselves. I assume your data is preprocessed so that each row corresponds to a PTM. You replace dpcQuant() with…
Votes
Answer: What R/Bioconductor tools would you recommend for the analysis of sncRNA, specif
Using edgeR or DESeq2 to analyze allele-specific expression?
Answer: DESeq2 design for haplotype MPRA
Answer: Failure to download resources (MeSHDb) from AnnotationHub
Answer: Failure to download resources (MeSHDb) from AnnotationHub
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