Dear Dr. Chris,
I am not getting proper alignment of peaks across samples. Same peak within the 
set parameters (mz tolerance=0.01 or 5ppm and RT tolerance=1.0 min, RT after 
correction=0.5 min) appears in 2-3 rows.
For example 145.0645 appears in 3 rows at 12.2 (detected in 3 samples out of 
20), 12.46 (detected in 5), 12.52 (detected in 6 samples) which are within RT 
tolerance. In other samples, it is not detected after alignment but is present 
in all the 20 deconvoluted peak list and also in original raw files within the 
RT deviation.
I don't understand about threshold value. When I give threshold value= RT 
tolerance (ex, 1.00 min in my case), I observe many of the peaks aligned as 
shown in the preview but I don't see such alignment in the aligned peak list.
With threshold value <1.0 min, I don't see peak alignment in the preview also.
My flow of work is as follows
mzXML files import(20 files)>baseline correction>MASS detection(centroid) > 
chromatogram builder > deconvolution (wavelets_XCMS) >deisotoping and filtering 
> RANSAC alignment. I have also sent my files using dropsend for your reference
I am using mzmine2 for metabolomics with LC-LTQ-Orbitrap at 60,000 resolution. 
Max RT deviation observed is <1.0 min.
I tried with several parameters in permutation and combination but nothing 
worked.
I am struck with this project since more than 15 days. I appreciate your early 
response
with regards

Raghavendra Gunnaiah
Ph.D Scholar
R1-013,Department of Plant Science
McGill University Macdonald Campus
21,111 Lakeshore Road
Ste. Anne de Bellevue, QC H9X 3V9

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