Dear all

I am quantifying an iTRAQ run, where one of the channel seems to be having 
lower intensity across the board (around 20%).  I am thinking of the TIC 
normalization (total intensity), but it is mentioned as "not recommended" 
in LIBRA settings. 

Why is it so? If I am mixing equal labelled peptide, what is wrong in TIC, 
assuming one of the peptides labeled poorly?  What is the alternative here 
if that is not suitable? 

Why is it so? If I am mixing equal labelled peptide, what is wrong in TIC, 
assuming one of the peptides labeled poorly?  What is the alternative here 
if that is not suitable?

*Also,* *Can I see the total intensity of each channel somewhere?*

Regards
Debojyoti

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