Peak labels (continued) centroid 3-56chromatogram, setting 3-54custom 3-61
custom, creating for fragment spectra 8-9
customizing 1-25
decimal places displayed 3-55,3-56
deleting from trace 3-44,3-59displaying 3-65
DNA C-5
extracting from DAT file 3-64factors affecting 3-52height 3-55,3-56horizontal 3-55,3-58immonium ions C-9manually applying 3-39,3-52manually inserting peaks 3-39monoisotopic 3-43
not displayed 3-59,3-66,9-14,9-15
overlapping 3-55,3-58peak start and end,
displaying 3-55,3-58PSD 8-8
RNA C-5
spectrum number 3-55,3-56spectrum, setting 3-56time 3-55,3-56troubleshooting 9-14turning on and off in
chromatogram 3-52user defined 3-61vertical 3-55,3-58
Vial number 3-55Peak labels, charge state
filtering 3-43incorrect 9-20not displayed 9-19parameters used 3-53requirements 3-53selecting 3-58
user labels 3-62
Peak labels, filtering charge state 3-43monoisotopic peak 3-43
Peak labels, Mass Difference From Adjacent Peak (regular
labels) 3-57From Adjacent Peak (user
labels) 3-62From Selected Peak 3-57
Peak list
charge state, displaying selected 3-42
Chro and Spec 3-40contents 3-38
copying apex masses only 1-41copying centroid masses only 1-41copying to Windows clipboard 1-40copying with headings 1-40copying without headings 3-41deleting peaks 3-44,3-59description 3-37
displaying 3-37,3-40filtering 3-43
importing and saving in Excel 3-41inserting peaks manually 3-39monoisotopic peaks,
displaying 3-42printing 3-44
saving as a file 3-40sorting 3-42
when created 3-37
zero charge state displayed 3-43Peak matches
clearing list 5-13,8-15sorting 5-11
Peak matching
automatic calibration 5-32manual calibration 5-6,5-9PSD calibration 8-14
Peak resolution, see Resolution, mass Peak Threshold%, replaced by %Base
Peak Intensity 3-20,3-22
