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FlowCytometryData
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FIXED: Using read.flowSet, getting a "no matching files found" error
flowCore
FlowCytometryData
2.0 years ago
hamiltond
▴ 10
0
votes
1
reply
818
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Undefined columns error R cytometry analysis
flowCore
ggcyto
FlowCytometryData
updated 2.5 years ago by
Jiang, Mike
★ 1.3k • written 2.9 years ago by
Elizabeth
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0
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0
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689
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Error in the use of flowTrans: L-BFGS-B needs finite values of 'fn'
flowCore
FlowCytometryData
flowTrans
flow
24 months ago
hamiltond
▴ 10
0
votes
0
replies
515
views
Error in set[, param[pcom[k, ]]] : subscript out of bounds
FlowCytometryData
Phenoflow
2.7 years ago
cy117
• 0
0
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0
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205
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News:
Online course - FLOW CYTOMETRY DATA ANALYSIS WITH R/BIOCONDUCTOR
Bioconductor
FlowCytometryData
FlowCytometry
3 months ago
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Answer: New genes that did not exist in dds object suddenly showed up after degPatterns
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Michael Love
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May be documented by the software you are using? https://github.com/lpantano/DEGreport
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Take a look at our workflow, this starts from a beginner's level. You could export from Excel using CSV or TSV, then read into R. htt…
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This support site is meant to help people with questions about Bioconductor packages (WGCNA is not a Bioconductor package). You might try o…
Comment: miRTarRnaseq library
by
mercedeh.movassagh
▴ 10
Yes that is correct
Comment: What benchmark should I use for setting the EdgeR filterByExpr min.count paramet
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Gordon Smyth
50k
It is the minimum group size rather than the total number of samples that is relevant. `min.prop` is more a biological parameter rather th…
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A: Error object and replacement value dimnames differ, when changing column names o
Comment: What benchmark should I use for setting the EdgeR filterByExpr min.count paramet
Comment: What benchmark should I use for setting the EdgeR filterByExpr min.count paramet
DESeq2 normalization vs VST vs rlog
Answer: DESeq2 "Contrast" option
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