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This example is currently in draft.

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. 


Dataset wrap
Namegf


Rowcaps


Row 1:

Shows the number of sequence variants variants within the region of interest.

Row 2:

Shows the normalized number of sequence variants variants within the region of interest. The formula applied for normalization is shown in GFANMETH.

Row 3:Shows the a summary of the magnitude of the variant burden within the tumor.



Dataset2


STUDYIDDOMAINUSUBJIDSPDEVIDGFSEQGFREFIDGFTESTCDGFTESTGFTSTDTLGFORRESGFORRESUGFSTRESCGFSTRESNGFSTRESUGFGENREFGFNAMGFSPECGFMETHODGFANMETHVISITNUMVISITVISITDYGFDTCGFDY
ABC-123GFABC123-45-001ACME 500 GENE PANEL
19675785578975864TMBTumor Mutation BurdenNORMALIZED NUMBER OF SEQUENCE VARIANTS8.83/MBP8.838.83497
497497/MBP
GRCh37.75ACME Genetics Inc.Lab PlusctDNANEXT GENERATION TARGETED SEQUENCINGDNAWHOLE EXOME SEQUENCINGUniform TMB Calculation Method Merino et al 2020 FORMULA
1SCREENING<ADD HERE><ADD HERE><ADD HERE>
ABC-123GFABC123-45-001ACME 500 GENE PANEL296757855TMBTumor Mutation BurdenVARIANT SEQUENCE BURDEN INTERPRETATIONintermediateNORMALIZED NUMBER OF SEQUENCE VARIANTS8.83/MBP8.838.83/MBPintermediateGRCh37.75ACME Genetics Inc.ctDNANEXT GENERATION TARGETED SEQUENCINGUniform TMB Calculation Method Merino et al 2020 FORMULA1SCREENING<ADD HERE><ADD HERE><ADD HERE>
ABC-123GFABC123-45-001ACME 500 GENE PANEL37897586496757855TMBTumor Mutation BurdenNUMBER OF VARIANT SEQUENCE VARIANTSBURDEN INTERPRETATION497intermediate497
497intermediate

GRCh37.75ACME Genetics Lab PlusInc.DNActDNANEXT GENERATION TARGETED WHOLE EXOME SEQUENCING
1SCREENING<ADD HERE><ADD HERE><ADD HERE>



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