A private company has done a microarray bioinformatic analysis with 2 close-related bacteria (TIGR4 and R6) under 2 different conditions (C and DFO)
> targets numero FileName Cy3 Cy5 A 1 A.txt R6C R6DFO B 2 B.txt R6DFO R6C C 3 C.txt TIGR4DFO R6DFO D 4 D.txt R6DFO TIGR4DFO E 5 E.txt TIGR4C TIGR4DFO F 6 F.txt TIGR4DFO TIGR4C G 7 G.txt R6C TIGR4C H 8 H.txt TIGR4C R6C
They did the limma analysis through a "separate channel" approach.
I am wondering if this "separate channel" analysis can be done with this experimental design or not
I mention this because i did myself a "Direct Two Color" analysis, and the number of DE genes with p<0.05 obtained with the "separate channel" is substantially higher than when the direct design is used
You are right. The design was done in a time where the company was able to convince my colleague to run the experiment this way. These two bacteria share a very high degree of conservation at the genomic sequence
However, my colleague is only interested in comparing the C and DFO conditions within a determined bacteria strain.
I think I will go by analyzing the A, B, E and F arrays through separate channels
Looks like a circular design to me with dye sways?