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readqpcr
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Incompatible phenoData object error in ReadqPCR package
ReadqPCR
phenoData object
4.9 years ago
jchoza
• 0
0
votes
0
replies
2.1k
views
reading qRT-PCR data
ddCt
HTqPCR
ReadqPCR
ddCt
HTqPCR
ReadqPCR
10.0 years ago
Guest User
★ 13k
0
votes
2
replies
3.1k
views
ReadqPCR: [[hkgs,]] incorrect number of dimensions
ReadqPCR
NormqPCR
ReadqPCR
NormqPCR
updated 11.2 years ago by
James Perkins
▴ 120 • written 11.2 years ago by
Guest User
★ 13k
0
votes
0
replies
1.1k
views
HTqPCR
convert
qpcrNorm
ddCt
HTqPCR
ReadqPCR
convert
qpcrNorm
ddCt
HTqPCR
ReadqPCR
11.2 years ago
Guest User
★ 13k
1
vote
1
reply
1.2k
views
qRT-PCR - reading tab-delimited file (biol & tech replicates)
qPCR
ReadqPCR
qPCR
ReadqPCR
11.3 years ago
boczniak767
▴ 720
0
votes
0
replies
1.1k
views
readQpcrBatch function in qpcrNorm
qpcrNorm
ReadqPCR
qpcrNorm
ReadqPCR
11.7 years ago
Mueller, Alan
▴ 20
0
votes
1
reply
1.2k
views
NormqPCR and ReadqPCR
GO
ReadqPCR
NormqPCR
GO
ReadqPCR
NormqPCR
updated 12.3 years ago by
james perkins
▴ 300 • written 12.3 years ago by
Pepijn Kooij
▴ 10
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Comment: Extremely small p-values using Limma for proteomic data
by
James W. MacDonald
65k
If you ever find yourself using the `@` function, you should reconsider what you are doing. There are vanishingly small instances when an e…
Comment: How to use bootRanges to bootstrap small RNA loci (nullranges package)
by
Michael Love
42k
Here is some example code <https://gist.github.com/mikelove/cbbc84634b6854c865cb5eb08ad9b245>
Comment: How to use spike-in information (sequences from another species) with DESeq2::DE
by
maria.soler
• 0
Hi, I have a question barely related to this topic. Do you use a custom reference genome combining your organism and the one used as a spik…
Answer: Differential gene expression analysis results
by
ATpoint
★ 4.1k
Pease do not open multiple posts for the same issue: https://support.bioconductor.org/p/9158194/#9158222 The support site is not meant f…
Comment: deseq2 results
by
sajadahmad41454
• 0
thank you for your response, should i remove or discard that sample? since the red outlier on left represents one of healthy samples.
Votes
Comment: Extremely small p-values using Limma for proteomic data
Comment: Log-cpm values from limma
Comment: Log-cpm values from limma
Comment: deseq2 results
Comment: deseq2 results
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