- click "Search->Settings", click "Load" and select "settings_histology.ini"
- fix path to the peaklists file "20170106_aspergill_s12R_converted_fwhm_0.050000.imzML"
- fix path to the compounds database file "sequencedatabase_ferricrocin.txt"
- click "Ok" to close the Settings dialog
- click "Search->Run"

- click "Tools->Summary Table of Matched Peaks", to see the results as reported in "output.csv"
- click "File->Export to CSV" to reproduce the file "output.csv"
- click "File->Export Statistics to CSV" to reproduce the file "output_statistics.csv"

- click "Tools->CrossVis"
- select "File->Open" and load the optical image of ITO MALDI plate "optical_image.jpg"
- select "File->Open" and load the histology image "histology_image.tif"
- set all the numbers as shown in "output_screenshot.png" to correlate the identified compounds 
with the optical image of ITO MALDI plate and with the histology image