[BioC] LIMMA: Unbalanced technical replicates
Gordon K Smyth
smyth at wehi.EDU.AU
Tue May 10 14:09:35 CEST 2005
> Date: Mon, 09 May 2005 16:34:02 +0300
> From: "Ron Ophir" <ron.ophir at weizmann.ac.il>
> Subject: [BioC] LIMMA: Unbalanced technical replicates
> To: <bioconductor at stat.math.ethz.ch>
>
> Hi,
> I have an affymetrix experiment with the following target file:
> Replicates FileName Target
> 8 SA100Hu133plus.CEL LR
> 4 SA101Hu133plus.CEL LR
> 4 SA102Hu133plus.CEL LR
> 4 SA103Hu133plus.CEL LR
> 9 SA104Hu133plus.CEL LR
> 5 SA105Hu133plus.CEL LR
> 5 SA106Hu133plus.CEL LR
> 10 SA107Hu133plus.CEL LR
> 11 SA108Hu133plus.CEL LR
> 12 SA109Hu133plus.CEL MET
> 13 SA111Hu133plus.CEL MET
> 14 SA112Hu133plus.CEL MET
> 15 SA113Hu133plus.CEL MET
> 16 SA114Hu133plus.CEL MET
> 17 SA115Hu133plus.CEL MET
> 18 SA116Hu133plus.CEL MET
> 6 SA117Hu133plus.CEL MET
> 6 SA119Hu133plus.CEL MET
> 19 SA121Hu133plus.CEL METD
> 20 SA122Hu133plus.CEL METD
> 7 SA123Hu133plus.CEL METD
> 7 SA124Hu133plus.CEL METD
> 21 SA127Hu133plus.CEL HR
> 1 SA83Hu133plus.CEL HR
> 1 SA84Hu133plus.CEL HR
> 1 SA85Hu133plus.CEL HR
> 22 SA86Hu133plus.CEL HR
> 2 SA87Hu133plus.CEL HR
> 2 SA88Hu133plus.CEL HR
> 2 SA89Hu133plus.CEL HR
> 23 SA90Hu133plus.CEL HR
> 3 SA92Hu133plus.CEL HR
> 3 SA93Hu133plus.CEL HR
> 24 SA94Hu133plus.CEL HR
> 25 SA95Hu133plus.CEL HR
> 26 SA96Hu133plus.CEL HR
> 27 SA98Hu133plus.CEL LR
> 28 SA99Hu133plus.CEL LR
> where files with the same number under replicates column are blocks of
> the technical replicates of the sames biological replicate.
> and the following design:
> LR HR MET METD
> SA100Hu133plus.CEL 1 0 0 0
> SA101Hu133plus.CEL 1 0 0 0
> SA102Hu133plus.CEL 1 0 0 0
> SA103Hu133plus.CEL 1 0 0 0
> SA104Hu133plus.CEL 1 0 0 0
> SA105Hu133plus.CEL 1 0 0 0
> SA106Hu133plus.CEL 1 0 0 0
> SA107Hu133plus.CEL 1 0 0 0
> SA108Hu133plus.CEL 1 0 0 0
> SA109Hu133plus.CEL 0 0 1 0
> SA111Hu133plus.CEL 0 0 1 0
> SA112Hu133plus.CEL 0 0 1 0
> SA113Hu133plus.CEL 0 0 1 0
> SA114Hu133plus.CEL 0 0 1 0
> SA115Hu133plus.CEL 0 0 1 0
> SA116Hu133plus.CEL 0 0 1 0
> SA117Hu133plus.CEL 0 0 1 0
> SA119Hu133plus.CEL 0 0 1 0
> SA121Hu133plus.CEL 0 0 0 1
> SA122Hu133plus.CEL 0 0 0 1
> SA123Hu133plus.CEL 0 0 0 1
> SA124Hu133plus.CEL 0 0 0 1
> SA127Hu133plus.CEL 0 1 0 0
> SA83Hu133plus.CEL 0 1 0 0
> SA84Hu133plus.CEL 0 1 0 0
> SA85Hu133plus.CEL 0 1 0 0
> SA86Hu133plus.CEL 0 1 0 0
> SA87Hu133plus.CEL 0 1 0 0
> SA88Hu133plus.CEL 0 1 0 0
> SA89Hu133plus.CEL 0 1 0 0
> SA90Hu133plus.CEL 0 1 0 0
> SA92Hu133plus.CEL 0 1 0 0
> SA93Hu133plus.CEL 0 1 0 0
> SA94Hu133plus.CEL 0 1 0 0
> SA95Hu133plus.CEL 0 1 0 0
> SA96Hu133plus.CEL 0 1 0 0
> SA98Hu133plus.CEL 1 0 0 0
> SA99Hu133plus.CEL 1 0 0 0
> My question is should I run duplicateCorrelation function with this
> vector
> B<-c( 8, 4, 4, 4, 9, 5, 5, 10, 11, 12, 13, 14, 15, 16, 17, 18,
> 6, 6, 19, 20, 7, 7, 21, 1, 11, 22, 2, 2, 2, 23, 3, 3, 24, 25,
> 26, 27, 28)
> where each biological replicate gets different block number
Yes.
> or
> B<-c( 4, 4, 4, 5, 5, 6, 6, 7, 7, 2, 2, 2, 3, 3, )
> where I ignore biological replicates or maybe put zero instead of
> biological replicates.
No.
> corfit <- duplicateCorrelation(data, design, block=B)
'block=targets$Replicate' would be fine.
Gordon
> Thanks
> Ron
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