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- Posts: 1
- Joined: Sat May 09, 2009 10:53 pm
I am using AMDIS to compare presence of a couple of analytes in some previously run Agilent files. I understand the mechanics of changes to the deconvolution settings (and I have read the users manual). What isn't covered is WHEN to alter the settings from default. I am tickled by the fact that I can completely reverse the relative concentrations (intg. sig) of my two target analytes, or even make the components disappear completely. I would appreciate a little practical wisdom or direction to such wisdom. Thanks for helping.
