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Non-hereditary solid tumor gene panel test (LiquidBiopsy)

GC Labs code	F081	Test Field	Human genetics
Compulsory forms	Oncology requisition and consent form, GC Genome Informed consent for genetic testing

GC Labs code

F081

Test Field

Human genetics

Compulsory forms

Oncology requisition and consent form, GC Genome Informed consent for genetic testing

Information

Test method	NGS (Next generation sequencing)
Specimen (mL)	WB 20.0 (exclusive container) Pleural fluid 20.0 (exclusive container)
Specimen storage	Ambient
Specimen stability	Ambient (7 days)
Test schedule	Mon-Fri
Analytical time (day)	14

Test method

NGS (Next generation sequencing)

Specimen (mL)

WB 20.0 (exclusive container)
Pleural fluid 20.0 (exclusive container)

Specimen storage

Ambient

Specimen stability

Ambient (7 days)

Test schedule

Mon-Fri

Analytical time (day)

Reference range/Unit	[Pleural Fluid] See comments in the report [Whole Blood] See comments in the report
Clinical Significance	As a test that analyzes genetic alteration of circulating tumor nucleic acid from a blood sample, it can help determine the treatment policy for malignant tumors. It can be applied to various malignant tumors such as stomach cancer, lung cancer, colon cancer, breast cancer, ovarian cancer, and prostate cancer. It can detect SNV, small indel, copy number variant, and gene rearrangement, and the detection limit of SNV and small indel mutations depends on the amount of DNA in the extracted sample.
Remark	Require to using Streak cell-free DNA tube for testing (cannot be performed with other tube & containers)

Reference range/Unit

 [Pleural Fluid]
See comments in the report

 [Whole Blood]
See comments in the report

Clinical Significance

As a test that analyzes genetic alteration of circulating tumor nucleic acid from a blood sample, it can help determine the treatment policy for malignant tumors. It can be applied to various malignant tumors such as stomach cancer, lung cancer, colon cancer, breast cancer, ovarian cancer, and prostate cancer. It can detect SNV, small indel, copy number variant, and gene rearrangement, and the detection limit of SNV and small indel mutations depends on the amount of DNA in the extracted sample.

Remark

Require to using Streak cell-free DNA tube for testing (cannot be performed with other tube & containers)