Good Morning,

 

I am writing to ask some advice. We are presently printing a 39,000 feature
array and I need some help. We are printing with the triplicates in the same
block and I cannot figure out how to get them out of the same block. It is
making limma analysis very difficult as the program seems to be designed to
analyze printed replicates in different blocks. Can anyone help me in
figuring out how to arrange my 96-well plates of oligos and or a get around
for limma?

 

Thank you for your help,

 

Liz Brooke-Powell 

 

Washington University Medical School, 

Department of Molecular Microbiology,

CB#8230, 660 S. Euclid Ave

St. Louis, MO, 63110 


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