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Tags: FISH, EGFR, Cytogenetic, cytogenetics

This example is currently in draft.


This example shows findings from a cytogenetic assessment of EGFR gene copy number amplification with the purpose of determining the diagnostic status of patients with non-small cell lung cancer. In this example, the findings are generated using fluorescence in situ hybridization (FISH) methodology and semi-quantitative microscopic assessment by a pathologist. Microscopic assessments are then summarized to a diagnostic status using a specific algorithm represented in GFANMTH.


Units need to be confirmed. Should we have a value for chromosome. GENSR is this applicable or needed (e.g., for exon)

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gf.xpt

gf.xpt

RowSTUDYIDDOMAINUSUBJIDGFSEQGFREFIDGFTESTCDGFTESTGFTSTDTLGFORRESGFORRESUGFSTRESCGFSTRESNGFSTRESUGFCHROMGFSYMGFSYMTYPGFGENSRGFSTATGFREASNDGFNAMGFSPECGFMETHODGFANMETHVISITNUMVISITVISITDYGFDTCGFDY
1ABC0023GFAB23-001145785-01CPNUMAMPCopy Number AmplificationCOPY NUMBER RATIO1.1
1.11.1

EGFRGENE WITH PROTEIN PRODUCT


ACME GENOMICS LABSDNAFISH
-1SCREENING-26/21/2023-1
2ABC0023GFAB23-001245785-01CPNUMAMPCopy Number AmplificationDETECTIONNEGATIVE
NEGATIVE


EGFRGENE WITH PROTEIN PRODUCT


ACME GENOMICS LABSDNAFISHCOLORADO SCORING METHOD FOR EGFR GENE AMPLIFICATION 2009 ALGORITHM-1SCREENING-26/21/2023-1
3ABC0023GFAB23-001345785-01CPNUMAMPCopy Number AmplificationCENTROMERE SIGNALS147PLACEHOLDER147147PLACEHOLDER
EGFRGENE WITH PROTEIN PRODUCT


ACME GENOMICS LABSDNAFISH
-1SCREENING-26/21/2023-1
4ABC0023GFAB23-001445785-01CPNUMAMPCopy Number AmplificationGENOME-SPECIFIC TARGET SIGNALS166PLACEHOLDER166166PLACEHOLDER
EGFRGENE WITH PROTEIN PRODUCT


ACME GENOMICS LABSDNAFISH
-1SCREENING-26/21/2023-1
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