To whom it may concerns,
I'm currently using mzmine software to exact ion chromatograph
from LC-MS data. I first ran the Chromatogram builder algorithm to
detect chromatograph then did deconvolution of chromatograms after
peak detction. One of problem is I found multiple peaks with same m/z
ratio in the peak list but with different RT, height and Area etc.
Because my data came from high-resolution mass spec with high-mass
accruracy, I would like to see one peak corresponding to one m/z ratio
in the peak list. So I was wandering if there is anything wrong in
what I did for XIC. Thanks!
chunchao
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