Obtaining Customer Training Information

To obtain Applied Biosystems training information, go to www.appliedbiosystems.com, click Services & Support at the top of the screen, then click Training.

I

Accessing files 1-6 Adjusting parameters

analysis 4-5 processing 4-5

report format 3-4, 4-18 Analysis

background 2-19 overview 2-2

parameters, types of 1-3 using default parameters 2-3 using group parameters 2-19 using individual parameters 2-19 Analysis parameters

accessing 1-6 adjusting 2-8 changing 1-5

copying from another data file 2-18 copying from GRO to MET 4-20 default analysis 2-3

definition 1-3 embedded 1-4

not saved as stand-alone files 1-7 replacing 2-18

resetting default 1-9 saving adjusted 2-18

when used from group file and data file 4-21

Analysis Parameters file (.ANP) 1-8 Analysis sections 1-8

Area Threshold 4-5

Associating areas with levels 4-14 Audit Trail feature 2-18

B

B* file see Data files Background analysis 2-19

Baseline noise integrated as peaks 2-6 Baseline timed events see Timed

events BioCAD software 1-6 Bunching Factor

adjusting 2-12 definition 2-12

C

Calibration curves

areas, generating 4-9

copying from another method 2-18 copying from group file 4-20 creating 1-5

displaying 4-12 generating 4-1, 4-14 levels, entering 4-10 results files for 4-9 Calibration parameters

adjusting 4-5 definition 1-3

resetting defaults 4-4

Calibration standards, preparing for Getting Started exercise 4-2 Calibration table, adding rows to 4-11 Certificates of analysis

obtaining A-8

Changes to Data Analysis Software Version 3.0 1-8

Index

D E X

N

scaling in reports 3-12 zooming in on 2-6, 2-10, 2-11 Columns, report

adding 3-6 deleting 3-5

Component Name dialog box 3-6 Components

amounts, entering 4-10 Components dialog box 4-10 information, entering 4-7 names, entering 4-7

Copying analysis/report parameters from group to data files 4-19 Copying parameters from one data file

to another 2-18 Curve fit type 4-11

Customer training, information A-10 Customizing reports 3-4

D

Data Analysis module

accessing from Control Panel 2-4 accessing from Group Analysis 2-4 ANP file not supported 1-8

before opening 1-6 definition 1-3

differences from Turbochrom 1-8 opening files in 1-6, 1-8

restrictions 1-6 software, parts of 1-3 version 3.0 changes 1-8 Data channels A, B, and C 1-8 Data files (.B*)

adjusting calibration parameters 4-5 adjusting processing

parameters 2-8, 4-5

analyzing 2-4

assigning calibration parameters 4-10 opening 1-6

provided with system 1-9

provided with system, opening 1-6 Data integration 2-2

Data Rate field 2-13

Default analysis and report parameters, resetting 1-9

Default Report example 3-4 Deleting columns from a report

format 3-5 Deleting events 2-15

Differences from Turbochrom software 1-8

Disabling peak detection for a section of the chromatogram 2-14 Documentation feature 2-18

E

Embedded parameters 1-4

Entering component information 4-7

F

Field Service in North America, contacting A-3

File types

and section types 1-5 functions of 1-3 not in Version 3.0 1-8

Footer, changing in a report format 3-6 Forced baselines 2-14

Forcing integration of undetected peaks 2-14

I

Generate a separate replot selection 3-12 Generating

calibration curves 4-14 reports 3-3

results files 4-9 Graphic Method Editor

accessing 4-2

analysis parameters, adjusting 2-8 opening additional files from 2-7 overview 1-5

techniques for use 2-2 timed events, setting 2-14 Group Analysis

definition 1-3 group analysis 2-19 individual analysis 2-19 Group files (.GRO)

copying parameters to MET file 4-20

opening 1-6

provided with system 1-9

saving CFG and MET information to stand-alone MET 4-20

H

Height of chromatogram plot, controlling 3-11

I

Incompatible files, using on different workstations 1-9

INTEGRAL software 1-6

Integration parameters, adjusting 2-8

L

Levels, associating with areas 4-14

M

Manipulating a chromatogram 1-5 Manual Calibration dialog box 4-14 Manual integration 2-14

Method files (.MET)

and analysis parameters 2-2 contents 1-4, 1-8

creating for unknowns 4-20 creating from a group file 4-20 opening 1-6

restrictions 1-9

to acquire unknowns 4-20 MSDSs, obtaining A-8

MTH see Analysis parameters

N

New method files, creating from group files 4-20

Noise integrated as peaks 2-6 Noise Threshold 4-5

Numeric labels at top of chromatogram 2-6

O

Open dialog box 2-5 Opening

data files 1-6, 1-8

files, from within Graphic Method Editor 2-7

method files 1-6

D E X

N

creating method file for unknowns 4-20 data analysis software 1-3 generating calibration curves 4-2 generating reports 3-2

Getting Started Guide 1-2 graphic method editor 1-5 quantitation of unknowns 4-2 report format editor 1-5 text method editor 1-5

P

Parameters

see also Analysis parameters see also Calibration parameters see also Processing parameters see also Report format parameters stored as sections 1-7

types and descriptions 1-3 Peak detection, disabling and

enabling 2-14 names, entering 4-7 spurious, eliminating 2-8 undetected 2-12

Prerequisites for Getting Started Guide exercises 1-4

Printing reports 3-9

reports with results and chromatogram on one page 3-11

reports without chromatogram 3-10

copying from a group file 4-19 definition 1-3

replacing 2-18 resetting defaults 2-3

Q

Quantitation

creating method for 4-20 of unknowns 4-1, 4-21

R

RAW file

definition 2-6

not saved as stand-alone files 1-7 Replace Analysis/Report Format dialog

box 1-10 Replot dialog box 3-12

Replot size command, using to control chromatogram height 3-11 Report footer, changing 3-6 Report Format Editor

accessing 3-4, 4-3 adjusting parameters 3-4 dialog box 3-8

overview 1-5

using to customize reports 3-4, 4-18

Report format parameters adjusting 3-4, 4-18 changing 1-5 columns 3-6 definition 1-3 footer, changing 3-6

not saved as stand-alone files 1-7 resetting to defaults 1-9

saving 3-8

setting for printing 3-11

I D E X N

when used from group file and data file 4-21

Report title, changing 3-4 Reports

chromatogram 3-3

chromatogram, printing on same page as results 3-11 chromatogram, rescaling 3-12 chromatogram, suppressing

printing 3-10 columns 3-5, 3-6 customizing 3-4 Peak Report 2-8 printing 3-3 setting up 3-3

Rescaling a chromatogram before printing 3-12

Resetting default analysis and report parameters 1-9

Response 4-11 Results files (.RST)

accessing 1-6

creating for a calibration curve 4-14 generating 4-9

storage location 4-9 Rider peaks, skimming 2-14 RPT see Report format parameters

S

Sample files

compatibility 1-9

provided with system 1-9 unknowns 4-21

Sampling Rate field 2-13 Saving adjusted analysis

parameters 2-18

Saving report format parameters 3-8

Software

changes to version 3.0 1-8 differences from Turbochrom 1-8 overview 1-3

T

Technical documents, obtaining A-8 Technical support, contacting

Eastern Asia, China, Oceania A-5 Europe A-6

Japan A-7

Latin America A-7

telephone or fax in North America A-3 Text Method Editor

accessing 4-2 overview 1-5

using to associate peak areas with component levels 4-14 using to enter calibration levels and

component amounts 4-10 Thresholds

Turbochrom software 1-8

U

Undetected peaks

forcing integration of 2-14 resulting from high Bunching

Factor 2-12

D E X

N

Version 3.0 changes 1-8

Viewing multiple data channels 1-6 VISION software 1-6

W

Weighting 4-11

Windows operating system 1-4

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In document Data Analysis Software (Page 80-87)