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This example shows findings from an assessment of the number of mutations within a tumor genome with the purpose of determining likely response to immunotherapy. (Need to add description here)a therapeutic agent and/or disease burden. In this example, findings are generated by two vendors using different methodologies and specimen types.


Dataset wrap
Namegf
Rowcaps
Row 1:

Shows the number of sequence variants within the region of interest. The vendor, methodology, and specimen type are shown in GFNAM, GFMETHOD, and GFSPEC. 

Row 2:

Shows the normalized number of sequence variants within the region of interest. The panel of genes used in next generation targeted sequencing is shown in SPDVID. The vendor, methodology, and specimen type are shown in GFNAM, GFMETHOD, and GFSPEC. 

Row 3:Shows the a summary of the magnitude of the variant burden within the tumor. The panel of genes used in next generation targeted sequencing is shown in SPDVID. The vendor, methodology, and specimen type are shown in GFNAM, GFMETHOD, and GFSPEC. 
Dataset2
RowSTUDYIDDOMAINUSUBJIDSPDEVIDGFSEQGFREFIDGFTESTCDGFTESTGFTSTDTLGFORRESGFORRESUGFSTRESCGFSTRESNGFSTRESUGFGENREFGFNAMGFSPECGFMETHOD
GFANMETH
VISITNUMVISITVISITDYGFDTCGFDY
1ABC-123GFABC123-45-001
ACME 500 GENE PANEL

1
96757855
78975864TMBTumor Mutation Burden
NORMALIZED
NUMBER OF SEQUENCE VARIANTS
8.83/MBP8.838.83
497
497497
/MBP

GRCh37.75
ACME
Genetics
Inc.
Lab Plus
ctDNANEXT GENERATION TARGETED SEQUENCINGUniform TMB Calculation Method Merino et al 2020 FORMULA
DNAWHOLE EXOME SEQUENCING1SCREENING
<ADD HERE><ADD HERE>
-12022-01-19-1
2
<ADD HERE>
ABC-123GFABC123-45-001ACME 500 GENE PANEL296757855TMBTumor Mutation Burden
VARIANT SEQUENCE BURDEN INTERPRETATIONintermediateintermediate
NORMALIZED NUMBER OF SEQUENCE VARIANTS8.83/MBP8.838.83/MBPGRCh37.75ACME Genetics Inc.ctDNANEXT GENERATION TARGETED SEQUENCING1SCREENING
-12022-01-19-1
3
<ADD HERE><ADD HERE><ADD HERE>
ABC-123GFABC123-45-001ACME 500 GENE PANEL3
78975864
96757855TMBTumor Mutation Burden
NUMBER OF
VARIANT SEQUENCE
VARIANTS
BURDEN INTERPRETATION
497
INTERMEDIATE
497497

INTERMEDIATE

GRCh37.75ACME Genetics
Lab Plus
Inc.
DNAWHOLE EXOME
ctDNANEXT GENERATION TARGETED SEQUENCING1SCREENING
<ADD HERE><ADD HERE><ADD HERE>
-12022-01-19-1