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This example shows a report table, trial design,

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and results data for the in vitro neutral red uptake (NRU) cytotoxicity assay
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in example study 123.

Expand
titleSample from Report Table

The following shows example data for study 123 in a report table. This report includes summary statistics (i.e., average, standard deviation, coefficient variation) for each plate and an EC50

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value for the entire value for the entire assay. In the table below, the light grey shading for plate 1 are values from wells that do not contain the NHK cells. The dark grey shading represents the column and row location within the 96-well plate, and in this example the applicant chose to use these column and row locations to assign their REFID values in the RELREF dataset and GT dataset.  

For brevity, the datasets in this example are not comprehensive but are intended to demonstrate a range of proper use. 


Neutral Red Cytotoxicity Assay Results (Relative Absorbance Data)




Sample ID

Smoke Regime

Replicate Number

Plate Number



Relative Assay Plate Absorbance Readings





Cigarette Smoke Condensate (µg/mL) 

SLS (µg/mL)


EC50 (µg/ml)

Well Column:

1

2

3

4

5

6

7

8

9

10

11

12


Well 
Row:

0

10

50

75

100

120

140

160

200

110

200

0



030001

Medium

1

1

A

0.046*

0.046*0.039*0.012*0.030*0.003*0.057*0.032*0.003*0.050*0.044*

0.040*



030001

Medium

1

1

B

0.048*

107

77.7

65.7

30.2

15.6

9.79

5.41

2.49

8.09

0.791

0.014*



030001

Medium

1

1

C

0.005*

98.6

77.4

57.7

35.8

8.09

7.36

3.22

0.791

6.38

0.061

0.050*



030001

Medium

1

1

D

0.049*

94.9

81.5

38.2

31.2

7.60

5.17

3.22

0.791

5.17

0.304

0.017*



030001

Medium

1

1

E

0.047*

111

78.1

64.5

32.9

8.82

5.90

2.74

1.28

10.3

0.547

0.011*



030001

Medium

1

1

F

0.032*

96.6

76.2

48.0

26.8

7.84

4.20

2.74

1.52

8.09

4.93

0.022*



030001

Medium

1

1

G

0.044*

105

77.9

58.2

28.3

8.09

4.68

1.76

0.547

8.57

1.76

0.056*



030001

Medium

1

1

H

0.056*

0.013*0.040*0.008*0.013*0.002*0.029*0.018*0.006*0.016*0.024*

0.046*


Average


101

78.2

54.5

29.9

9.70

6.17

3.37

1.19

8.94

1.22



Std. Dev.


6

2.9

9.4

3.6

2.95

2.19

1.12

0.72

2.72

1.58



Coeff. Var.


5.8

3.6

17.2

11.9

30.4

35.5

33.1

61.0

30.5

129.9



*media without cells















030001

Medium

1

2

A


93.4

74.0

56.0

35.1

11.8

8.70

5.10

1.98

5.34

1.02




030001

Medium

1

2

B


102

75.2

53.3

35.1

11.8

7.74

5.58

3.66

5.34

1.02




030001

Medium

1

2

C


107

79.0

55.0

26.5

10.1

6.06

3.66

1.74

7.02

0.780




030001

Medium

1

2

D


104

80.2

55.3

29.8

8.94

3.90

3.66

1.50

6.30

0.780




030001

Medium

1

2

E


101

75.7

54.1

26.7

4.86

4.38

1.26

1.02

6.30

1.02




030001

Medium

1

2

F


110

85.7

67.7

26.0

5.34

4.62

3.42

1.50

6.30

0.540




030001

Medium

1

2

G


104

77.8

64.9

27.7

8.22

3.18

2.46

1.02

6.30

0.780




030001

Medium

1

2

H


103

71.6

58.9

25.5

9.42

4.14

3.90

1.26

4.38

0.780



Average


103

77.4

58.1

29.0

8.82

5.34

3.63

1.71

5.91

0.840



Std. Dev.


5

4.4

5.3

4.0

2.63

1.97

1.37

0.86

0.83

0.170



Coeff. Var.


4.6

5.6

9.2

13.6

29.8

36.9

37.6

50.0

14.1

20.2



EC50 (µg/ml). Effective concentration at 50% cytotoxicity.  (using a specific sigmoidal equation = model). 













123

Dataset wrap
912  TOBA-56
Rowcaps
8 the applicant's
Rows 1-2:Show 2 records for TSPARMCD = "GLPTYP", using TSSEQ to indicate multiple records, since both GLP types apply for this example study. 
Row
3:Shows that
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this study was conducted as a GLP study.
Rows 4-5:Show the study start date and study title.
Rows 6-7:Show the version of SEND Implementation Guide and version of Controlled Terminology used in this study.
Row 8:Shows the applicant's organization.
Row 9:

Shows that the applicant's study reference ID is not applicable.

Rows
10-
13:Show that TSGRPID has been used to link records (name, location, country) related to the test facility (TSGRPID = 1). The study director is associated with the test facility.
Rows 14-16:

Show that TSGRPID (TSGRPID=4) has been used to link the information on the testing guideline followed on this study (TSTGDNAM, TSTGDORG, TSTGDVER).

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key

Row 17:

Shows the study type for this study.

Row 18:

Shows that this study includes a Neutral Red Uptake Assay.
Rows 19-20:Show that the species is human and the cell line is NHK in this study.
2022-05-25
Dataset2
Row

STUDYID

DOMAIN

TSSEQ

TSGRPID

TSPARMCD

TSPARM

TSVAL

TSVALNF

1123TS1
GLPTYPGood Laboratory Practice TypeFDA
2123TS2
GLPTYPGood Laboratory Practice TypeOECD
3123TS1
STSTDTCStudy Start Date

GLPFLGLP FlagY
4123TS1
STITLE

STSTDTCStudy Start Date2022-05-25
5123TS1
STITLEStudy Title

Determination of the in vitro genotoxicity potential using the in vitro Neutral Red Uptake assay

5

6123TS1
SNDIGVERSEND Implementation Guide VersionTOBACCO IMPLEMENTATION GUIDE VERSION 1.0
6

7123TS1
SNDCTVERSEND Controlled Terminology VersionSEND Terminology 2021-09-30
7

8123TS1
APPLCNTApplicant
Organization
Example Applicant Inc.
8

9123TS1
APREFIDApplicant Study Reference ID
NOT APPLICABLE
9
10123TS11TSTFNAMTest Facility NameExample Test Lab Name
10

11123TS11TSTFLOCTest Facility Location10 Somewhere Street, Montgomery, AL 10000
11

12123TS11TFCNTRYTest Facility CountryUSA
12

13123TS11STDIRStudy DirectorDr. R. Smith
13123TS1GLPFLGLP FlagY

14123TS14TSTGDNAMTesting Guideline NamePublication No. 07-4519
15123TS14TSTGDORGTesting Guideline OrganizationNIH
16123TS14TSTGDVERTesting Guideline Version2006-11
17123TS1
SSTYPStudy TypeGENOTOXICITY IN VITRO
18123TS1
GNTXAIDGenetic Toxicology Assay IdentifierNRU
19123TS1
SPECIESSpeciesHUMAN
20123TS1
CELLLNCell LineNHK
Dataset wrap
Rowcaps
Rows 1-12:Show the test conditions for the

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Rowcaps
Rows 1-12:Show the test conditions for the set with a short name or SETCD value of NRU. The applicant chose this value to represent test conditions for the entire assay. 
Rows 13-2031:Show the test conditions for the set with a short name or SETCD value of CSC-50b. The applicant chose this value to represent plate number 1, well row A, well column 3, with a concentration of 50µg/mLof cigarette smoke condensate as shown in the report table for study 123.  The value for Cell Line (CELLLN) is not applicable because the well is a media-only well, having no NHK cells.

Rows 2132-2850:

Show the test conditions for the set with a short name or SETCD value of CSC-50. The applicant chose this value to represent plate number 1, well rows B-G, well column 3 and plate number 2, well rows A-H, well column 3. These all have the concentration of 50µg/mLof cigarette smoke condensate as shown in the report table for study 123.
Rows 2951-3669:Show the test conditions for the set with a short name or SETCD value of SLS-110. The applicant chose this value to represent plate number 1, well rows B-G, well column 10, and plate number 2, well rows A-H, well column 10. These all have the concentration of 110µg/mLof sodium laurel sulfate as shown in the report table for study 123.
Dataset2
Row
ROWSTUDYIDDOMAINSETCDSETTXSEQTXPARMCDTXPARMTXVAL
1123TXNRUNRU_ASSAY1IVTDMINIn vitro Treatment Duration Minimum47.5
2123TXNRUNRU_ASSAY2IVTDTRGIn vitro Treatment Duration Target48
3123TXNRUNRU_ASSAY3IVTDMAXIn vitro Treatment Duration Maximum48.5
4123TXNRUNRU_ASSAY4IVTDUIn vitro Treatment Duration UnitHOURS
5123TXNRUNRU_ASSAY5INCBTMPIncubation Temperature37
6123TXNRUNRU_ASSAY6INCBTMPUIncubation Temperature UnitC
7123TXNRUNRU_ASSAY7SWAVENMSpectrophotometer Wavelength540
8123TXNRUNRU_ASSAY8ATMRHPAtmospheric Relative Humidity Percent90
9123TXNRUNRU_ASSAY9ATMCO2PAtmospheric CO2 Percent5
10123TXNRUNRU_ASSAY10SPDEVIDapplicant defined device identifierPUFFMASTER3k
11123TXNRUNRU_ASSAY11SMKRGMSmoking RegimenMEDIUM INTENSITY REGIMEN
12123TXNRUNRU_ASSAY12SPTOBID

Applicant-defined tobacco identifier

CIG01a
13123TXCSC-50bCSC-50-blank13
PSETCD

Parent Set Code

IVTDMINIn vitro Treatment Duration Minimum47.5
NRU
14123TXCSC-50bCSC-50-blank14
EXPTYP

Exposure Type

IVTDTRGIn vitro Treatment Duration Target48
Air Liquid Interface
15123TXCSC-50bCSC-50-blank15
SAMTYPSample Type
IVTDMAXIn vitro Treatment Duration Maximum48.5
Whole Smoke Conditioned Media
16123TXCSC-50bCSC-50-blank16
ITVNAMName of the Intervention Article
IVTDUIn vitro Treatment Duration UnitHOURS
Tobacco ProdA
17123TXCSC-50bCSC-50-blank17
ITVTYPEIntervention Article Type
INCBTMPIncubation Temperature37
PRODUCT
18123TXCSC-50bCSC-50-blank18
ITVCONC

Intervention Article Concentration

INCBTMPUIncubation Temperature UnitC
50
19123TXCSC-50bCSC-50-blank19
ITVCONCUIntervention Article Concentration Unit
SWAVENMSpectrophotometer Wavelength540
ug/ml
20123TXCSC-50bCSC-50-blank20
CELLLNCell Line
ATMRHPAtmospheric Relative Humidity Percent90
NOT APPLICABLE
21123TXCSC-
50
50bCSC-50-blank21
PSETCD

Parent Set Code

ATMCO2PAtmospheric CO2 Percent5
NRU
22123TXCSC-
50
50bCSC-50-blank22
EXPTYP

Exposure Type

SPDEVIDapplicant defined device identifierPUFFMASTER3k
Air Liquid Interface
23123TXCSC-
50
50bCSC-50-blank23
SAMTYP
SMKRGM
Sample Type
Smoking RegimenMEDIUM INTENSITY REGIMEN
Whole Smoke Conditioned Media
24123TXCSC-
50
50bCSC-50-blank24
ITVNAMIntervention Article Name
SPTOBID

Applicant-defined tobacco identifier

CIG01a
Tobacco ProdA
25123TXCSC-
50
50bCSC-50-blank25
ITVTYPE
EXPTYP
Intervention Article

Exposure Type

PRODUCT
Air Liquid Interface
26123TXCSC-
50
50bCSC-50-blank26
ITVCONC

Intervention Article Concentration

SAMTYPSample TypeWhole Smoke Conditioned Media
50
27123TXCSC-
50
50bCSC-50-blank27
ITVCONCU
ITVNAMName of the Intervention Article
Concentration Unitug/ml
Tobacco ProdA
28123TXCSC-
50
50bCSC-50-blank28
CELLLNCell Line
ITVTYPEIntervention Article TypePRODUCT
NHK
29123TX
SLS
CSC-
110
50b
SLS
CSC-50-
110
blank29
PSETCD

Parent Set Code

ITVCONC

Intervention Article Concentration

50
NRU
30123TX
SLS
CSC-
110
50b
SLS
CSC-50-
110
blank30
EXPTYP

Exposure Type

ITVCONCUIntervention Article Concentration Unitug/ml
Air Liquid Interface
31123TX
SLS
CSC-
110
50b
SLS
CSC-50-
110
blank31
SAMTYP
CELLLN
Sample Type
Cell LineNOT APPLICABLE
Liquid
32123TX
SLS
CSC-
110
50
SLS
CSC-
110
5032
ITVNAMIntervention Article Name
IVTDMINIn vitro Treatment Duration Minimum47.5
Sodium Laurel Sulfate
33123TX
SLS
CSC-
110
50
SLS
CSC-
110
5033
ITVTYPEIntervention Article Type
IVTDTRGIn vitro Treatment Duration Target48
POSITIVE CONTROL
34123TX
SLS
CSC-
110
50
SLS
CSC-
110
5034
ITVCONC

Intervention Article Concentration

IVTDMAXIn vitro Treatment Duration Maximum48.5
110
35123TX
SLS
CSC-
110
50
SLS
CSC-
110
5035
ITVCONCUIntervention Article Concentration Unit
IVTDUIn vitro Treatment Duration UnitHOURS
ug/ml
36123TX
SLS
CSC-
110
50
SLS
CSC-
110
5036
CELLLN
INCBTMP
Cell Line
Incubation Temperature
NHK
37
37123TXCSC-50CSC-5037INCBTMPUIncubation Temperature UnitC
38123TXCSC-50CSC-5038SWAVENMSpectrophotometer Wavelength540
39123TXCSC-50CSC-5039ATMRHPAtmospheric Relative Humidity Percent90
40123TXCSC-50CSC-5040ATMCO2PAtmospheric CO2 Percent5
41123TXCSC-50CSC-5041SPDEVIDapplicant defined device identifierPUFFMASTER3k
42123TXCSC-50CSC-5042SMKRGMSmoking RegimenMEDIUM INTENSITY REGIMEN
43123TXCSC-50CSC-5043SPTOBID

Applicant-defined tobacco identifier

CIG01a
44123TXCSC-50CSC-5044EXPTYP

Exposure Type

Air Liquid Interface
45123TXCSC-50CSC-5045SAMTYPSample TypeWhole Smoke Conditioned Media
46123TXCSC-50CSC-5046ITVNAMIntervention Article NameTobacco ProdA
47123TXCSC-50CSC-5047ITVTYPEIntervention Article TypePRODUCT
48123TXCSC-50CSC-5048ITVCONC

Intervention Article Concentration

50
49123TXCSC-50CSC-5049ITVCONCUIntervention Article Concentration Unitug/ml
50123TXCSC-50CSC-5050CELLLNCell LineNHK
51123TXSLS-110SLS-11051IVTDMINIn vitro Treatment Duration Minimum47.5
52123TXSLS-110SLS-11052IVTDTRGIn vitro Treatment Duration Target48
53123TXSLS-110SLS-11053IVTDMAXIn vitro Treatment Duration Maximum48.5
54123TXSLS-110SLS-11054IVTDUIn vitro Treatment Duration UnitHOURS
55123TXSLS-110SLS-11055INCBTMPIncubation Temperature37
56123TXSLS-110SLS-11056INCBTMPUIncubation Temperature UnitC
57123TXSLS-110SLS-11057SWAVENMSpectrophotometer Wavelength540
58123TXSLS-110SLS-11058ATMRHPAtmospheric Relative Humidity Percent90
59123TXSLS-110SLS-11059ATMCO2PAtmospheric CO2 Percent5
60123TXSLS-110SLS-11060SPDEVIDapplicant defined device identifierPUFFMASTER3k
61123TXSLS-110SLS-11061SMKRGMSmoking RegimenMEDIUM INTENSITY REGIMEN
62123TXSLS-110SLS-11062SPTOBID

Applicant-defined tobacco identifier

CIG01a
63123TXSLS-110SLS-11063EXPTYP

Exposure Type

Air Liquid Interface
64123TXSLS-110SLS-11064SAMTYPSample TypeLiquid
65123TXSLS-110SLS-11065ITVNAMIntervention Article NameSodium Laurel Sulfate
66123TXSLS-110SLS-11066ITVTYPEIntervention Article TypePOSITIVE CONTROL
67123TXSLS-110SLS-11067ITVCONC

Intervention Article Concentration

110

68123TXSLS-110SLS-11068ITVCONCUIntervention Article Concentration Unitug/ml
69123TXSLS-110SLS-11069CELLLNCell LineNHK
EXPERIMENTAL UNIT
Dataset wrap
Namerelref

The applicant chose to define the REFID values to indicate the Plate, the Column, and the Row of the wells of the 96-well plate in use, such that the well on plate 2, column 10, row G would assigned a REFID of 2-10-G.

Dataset wrap
Namerelref

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Rowcaps
Row 1:Shows the REFID of 123NRU that indicates the entire assay.
Rows 2, 5, 8, 9:-4: Show the REFIDs at the second level, all within the parent assay of 123NRU (REFID values of 1-3b, 1-3, 1-10, 2-10) which have LVLDESC of OBSERVATIONAL UNITSUMMARY.  If this study had recorded summary statistics for an entire trial set (e.g., across both plates for the same dose level), there would be an additional REFID for the trial set (with a LVLDESC of TRIAL SET).
Rows 3-4, 6-7, 10-11: Show REFID values that the applicant chose, in this case, to represent the plate number (1 or 2), column (1 - 12), and row (A-G) of the 96-well plates.
(e.g., across both plates for the same dose level), there would be an additional REFID for the trial set (with a LVLDESC of TRIAL SET).
Rows 5-6Rows 3-4:Show the REFIDs 1-3-A and 1-3-H that indicate two experimental units that are also observational units within the SETCD of CSC-50b that have the parent trial set of 1-3bREFID of 123NRU.
Rows 67-78:Show the REFIDs 1-3-B and 1-3-C that indicate two experimental units that are also observational units within the parent trial set SETCD of CSC-50 that have the parent REFID of 1-3.
Row 109:Shows the REFID of 1-10-G that indicates the experimental unit that is also an observational unit within the parent trial set SETCD of SLS-110 that has the parent REFID of 1-10.
Row 1110Shows the REFID of 2-10-G that indicates the experimental unit that is also an observational unit within the SETCD of SLS-110 that has the parent trial set REFID of 2-10.
1-3-A
Dataset2
tableidrelref
Row

STUDYID

SETCD

REFID

PARENT

LEVEL

LVLDESC

1123

NRU

123NRU
1ASSAY
2123CSC-
50b
501-
3b
3123NRU2OBSERVATIONAL
UNIT
SUMMARY
3123

CSC-50b

SLS-1101-
3b
10123NRU
3
2
EXPERIMENTAL UNIT
OBSERVATIONAL SUMMARY
4123
CSC
SLS-
50b
110
1
2-
3-H
1-3b3
10123NRU2OBSERVATIONAL SUMMARY
5123

CSC-

50

50b

1-3-A

123NRU

2EXPERIMENTAL UNIT/OBSERVATIONAL UNIT
6123

CSC-

50

50b

1-3-
B
H
1-3
123NRU
3
2EXPERIMENTAL UNIT/OBSERVATIONAL UNIT
7123CSC-501-3-
C
B1-33EXPERIMENTAL UNIT
8123SLS-1101-10123NRU2
/OBSERVATIONAL UNIT
9
8123
SLS
CSC-
110
50
2
1-3-
10
C
123NRU
1-3
2
3EXPERIMENTAL UNIT/OBSERVATIONAL UNIT
10
9123SLS-1101-10-G1-103EXPERIMENTAL UNIT/OBSERVATIONAL UNIT
11
10123SLS-1102-10-G2-103EXPERIMENTAL UNIT/OBSERVATIONAL UNIT