Showing : illuminahumanmethylation450k.db • reset
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Illumina 450k Manifest: Probes Mapping to Multiple RefGene Groups and Names
illuminahumanmethylation450kanno.ilmn12.hg19 minfi illuminahumanmethylation450k.db methylation
updated 13 months ago by • 0 • written 7.7 years ago by ▴ 10
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Using topGO for GO Enrichment on methylation markers (Illumina 450k)
topGO illuminahumanmethylation450k.db
5.2 years ago dusan.petrovic • 0
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Error while using ChAMP
champ methylation illuminahumanmethylation450k.db illumina450k
updated 6.5 years ago by ▴ 90 • written 6.5 years ago by ▴ 20
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Aclust package: IlluminaHumanMethylation450kCHR37 not found
illuminahumanmethylation450k.db aclust methylation annotation illumina
updated 6.7 years ago by • 0 • written 6.8 years ago by • 0
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install IlluminaHumanMethylation450k.db error
illuminahumanmethylation450k.db
updated 7.0 years ago by 25k • written 7.0 years ago by ▴ 190
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Illumina MethylationEPIC vs. 450K
methylumi minfi illuminahumanmethylation450k.db 450k methyanalysis
updated 7.3 years ago by ▴ 650 • written 7.3 years ago by ▴ 50
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error nonzero exit
illuminahumanmethylation450k.db rnbeads
updated 7.3 years ago by • 0 • written 7.8 years ago by • 0
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12
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4.8k
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‘IlluminaHumanMethylation450k.db’ had non-zero exit status
IlluminaHumanMethylation450k.db
updated 7.3 years ago by • 0 • written 8.6 years ago by • 0
2
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3
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1.7k
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IlluminaHumanMethylation450k.db installation error
IlluminaHumanMethylation450k.db
updated 7.4 years ago by ★ 8.2k • written 7.4 years ago by ▴ 180
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4
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preprocessFunnorm in minfi
minfi 450k illuminahumanmethylation450k.db normalization
updated 7.5 years ago by 63k • written 7.5 years ago by • 0
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1.8k
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IlluminaHumanMethylation450k.db - error on trying to insall
IlluminaHumanMethylation450k.db
7.6 years ago Brian Smith ▴ 120
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1.7k
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minfi - estimatecellcount function
minfi illuminahumanmethylation450kanno.ilmn12.hg19 illuminahumanmethylation450k.db
updated 7.8 years ago by 6.5k • written 7.8 years ago by ▴ 60
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Interepretation of dmpFinder result in minfi
microarray illuminahumanmethylation450k.db minfi
7.8 years ago ankita.chatterjee88 • 0
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Removing sex-chromosome probes from methyLumiSet
methylumi eSet illuminahumanmethylation450k.db featureFilter
updated 7.9 years ago by 63k • written 7.9 years ago by • 0
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Analyzing 450k Methylation from TCGA Website
minfidata minfi illuminahumanmethylation450k.db illuminahumanmethylation450kanno.ilmn12.hg19
8.1 years ago alejandretheodore • 0
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illumina 450k methylation: Cell composition for saliva
methylation minfi illuminahumanmethylation450k.db saliva cell composition
updated 8.2 years ago by 6.5k • written 8.2 years ago by ▴ 120
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Understanding methyAnalysis Results
methyAnalysis methyanalysis methylation illuminahumanmethylation450k.db
updated 8.2 years ago by ▴ 80 • written 8.2 years ago by ▴ 360
17 results • Page 1 of 1
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Comment: Question on constructing design matrix and defining contrasts for analysis by mohammedtoufiq91 ▴ 10
@gordonsmyth thank you, yes, please find the targets frame below. Basically, I want to create a design matrix and binarize by 0 and 1 to be…
Comment: WGCNA: many over and under-expressed features in modules of a signed network by andres.firrincieli ▴ 50
answered in Biostars: https://www.biostars.org/p/9564943/
Comment: Multitasking and Rbwa by Jean-Philippe Fortin • 0
Indeed, one can pass additional arguments to the `bwa_aln` function in `Rbwa`: bwa_aln(type="single", index_prefix=index_pr…
Comment: biomaRt error: database disk image is malformed by Emile • 0
UNBORKING the bioMaRt cache `biomaRt::biomartCacheClear()` also fixes the troubles with PANTHER.db installation which have also something t…
Answer: Proteomics data with NA values by Laurent Gatto 1.6k
- First, you need to assess how many missing values you have. - I would recommend not to impute your data by 0 (or any arbitrary small …
Votes
Answer: Question on constructing design matrix and defining contrasts for analysis
WGCNA: many over and under-expressed features in modules of a signed network
Comment: WGCNA: many over and under-expressed features in modules of a signed network
Answer: DESeq2 or edgeR for Presence and Absence of Proteins
Answer: Normalized counts from LRT or Wald test?
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