I

Detection Ranges (continued)

setting manually,

N

chromatogram 3-19,3-20

D

setting manually, spectrum 3-28

E

setting parameters globally,

spectrum 3-22

X

setting parameters locally,

 

spectrum 3-30

 

Detection, see Peak detection

 

 

DI in spectrum header 2-32,3-49

 

Diode array detector data, see DAD

 

Diode array detector data, see DAD

 

data

 

Disk space, conserving by converting

 

profile data to centroid 1-33

Display range scaling 2-11

xrange, expanding 2-11

yrange, expanding 2-11

Display Trace dialog box 2-18Displaying

peak labels 3-54,3-56

Voyager chromatogram window 2-7DNA residues, labeling C-5

Double bond equivalents (DBE) definition 6-6determining 6-6

Duplicating a trace 2-15

E

EF

in chromatogram header 2-30,4-25redisplaying original data 4-26

Elemental composition calculating 6-2description 6-2elements, adding 6-9fragment ions, electron state for

accurate results 6-5fragment ions, identifying 6-2

Elemental composition (continued) Isotope Match Score 6-6Isotope Match Score not reported

for fragment ion calculations 6-6

isotope min and max values ignored 6-8,6-11

limits, setting 6-7,6-9,6-12Periodic table 6-10procedure 6-3

results 6-5Elemental targeting

description 6-31

Isotope Match Score 6-33procedure 6-31

results 6-33

theoretical isotope, displaying 6-33Eliminate Fit Outlier 5-12

E-mail address, Technical Publications xiv

Equations

PSD calibration 8-6resolution-based peak

detection 3-4

Error, calibration fit 5-12initial 5-12

Event tag filtering (Mariner data only) not displayed on Process

menu 4-24

overview 4-23performing 4-24redisplaying original data 4-26

Event tag, MS Method (Mariner data only)

see also MS Method (Mariner data only), events

determining tags in file 4-23displaying 4-23

filtering 4-23

redisplaying original data 4-26 Examples, see Data Explorer examples

Index-10 Applied Biosystems