hi,
I have 2 RT-PCR microfluidics cards but done on different days:

- card A has 51 samples and 48 genes
- card B has 160 samples and 96 genes

They have in common 7 samples and 41 genes.  In both cards each gene is
measured in duplicate.

I might use HTqPCR functions for instance to analyze them.
But any hint about how can I merge the two cards in a single dataset in a
way to moderate/eliminate the putative day and card bias?

regards,
Alex


------------------------------------------------
Alessandro Brozzi,* *PhD
Department of Mathematics and Informatics
University of Perugia
via Vanvitelli, 1 06123 Perugia, ITALY
office n. 507
tel: +39 075 585 5039
mail: alessandro.brozzi[@]dmi.unipg.it

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