-
- Posts: 2
- Joined: Thu Jun 10, 2010 1:39 am
I have a couple of questions re: metabolomic data processing using AMDIS that I hope someone might be able to help with:
1. I would like to export .csv data (RI plus TIC or even indidual m/z areas or intensities) on all deconvoluted peaks (including unknowns), prior to annotating/matching each peak via a library? Does anyone know if this is possible? Does this make sense?
2. Apparently I should be able to change the processing method for individual chromatograms in a batch job, however, although I can select different processing methods, it does not seem to save, resulting in all chromatograms being processed by the 'simple' analysis type. Does anyone have any tips for me on how to overcome this?
Thank you very much for your help,
