Id e x n – HP Data Explorer 4 Series User Manual
Page 436
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Applied Biosystems
Peak labels (continued)
centroid 3-56
chromatogram, setting 3-54
custom 3-61
custom, creating for fragment
spectra 8-9
customizing 1-25
decimal places displayed 3-55,
deleting from trace 3-44, 3-59
displaying 3-65
DNA C-5
extracting from DAT file 3-64
factors affecting 3-52
height 3-55, 3-56
horizontal 3-55, 3-58
immonium ions C-9
manually applying 3-39, 3-52
manually inserting peaks 3-39
monoisotopic 3-43
not displayed 3-59, 3-66, 9-14,
overlapping 3-55, 3-58
peak start and end,
PSD 8-8
RNA C-5
spectrum number 3-55, 3-56
spectrum, setting 3-56
time 3-55, 3-56
troubleshooting 9-14
turning on and off in
chromatogram 3-52
user defined 3-61
vertical 3-55, 3-58
Vial number 3-55
Peak labels, charge state
filtering 3-43
incorrect 9-20
not displayed 9-19
parameters used 3-53
requirements 3-53
selecting 3-58
user labels 3-62
Peak labels, filtering
charge state 3-43
monoisotopic peak 3-43
Peak labels, Mass Difference
From Adjacent Peak (regular
labels) 3-57
From Adjacent Peak (user
labels) 3-62
From Selected Peak 3-57
Peak list
charge state, displaying
selected 3-42
Chro and Spec 3-40
contents 3-38
copying apex masses only 1-41
copying centroid masses only 1-41
copying to Windows clipboard 1-40
copying with headings 1-40
copying without headings 3-41
deleting peaks 3-44, 3-59
description 3-37
displaying 3-37, 3-40
filtering 3-43
importing and saving in Excel 3-41
inserting peaks manually 3-39
monoisotopic peaks,
displaying 3-42
printing 3-44
saving as a file 3-40
sorting 3-42
when created 3-37
zero charge state displayed 3-43
Peak matches
clearing list 5-13, 8-15
sorting 5-11
Peak matching
automatic calibration 5-32
manual calibration 5-6, 5-9
PSD calibration 8-14
Peak resolution, see Resolution, mass
Peak Threshold%, replaced by %Base