
National Association of Testing Authorities, Australia
Scope of Accreditation
Translational Genomics and Epigenomics Laboratory
Site
BEACON Biomarkers Laboratory-Austin
BEACON Biomarkers Laboratory
Accreditation No.
19912
Site No.
23962
Date of Accreditation
21 Dec 2017
Address
Level 8, Lance Townsend Building, Austin Hospital, 145 Studley Road
Heidelberg, VIC 3084
Australia
Contact
Availability
Services available to external clients
Supervision
Not Applicable
Scope of Accreditation
Withdrawn 12 Jan 2026
Voluntary
ISO 15189 (2012)
- This facility complies with the relevant National Pathology Accreditation Advisory Council (NPAAC) requirements.
Human Pathology
| Service | Product | Determinant |
|---|---|---|
| Molecular genetics - Assay for defined mutation or polymorphism (including pharmacogenetic testing) - Whole exome sequencing studies for inherited (germline) DNA/RNA changes | ||
| Molecular genetics - DNA sequencing | Blood; Extracted DNA; Formalin-fixed paraffin-embedded (FFPE) tissues; Tissues | DNA sequence analysis |
| Molecular genetics - Genetic testing for chimerism and mosaic gene variants (cancer and somatic mosaicism) - Targeted panels for non-inherited (somatic) DNA/RNA changes | Blood; Fluids; Formalin-fixed paraffin-embedded (FFPE) tissues; Plasma; Tissues | Blood borne tumours; Essential thrombocythemia (ET); Glioblastoma; Inherited cancer syndromes; MGMT promoter methylation analysis; MLH1 promoter methylation analysis; Nucleic acid analysis for specific variants; Polycythaemia vera; Primary myelofibrosis; Solid tumours |
| Molecular genetics - Investigation of constitutional genetic variants - Carrier testing - Targeted genes | Blood; Formalin-fixed paraffin-embedded (FFPE) tissues | Blood borne tumours; Inherited blood borne tumours; Inherited cancer syndromes; Nucleic acid analysis for specific variants; Nucleic acid analysis for unknown variants; Polycythaemia; Solid tumours |
| Molecular genetics - Predictive genetic testing - Targeted genes | Blood; Formalin-fixed paraffin-embedded (FFPE) tissues | Blood borne tumours; Breast cancer; Inherited blood borne tumours; Inherited cancer syndromes; Inherited colorectal cancer; Inherited disorders; Inherited solid tumours; Solid tumours |
| Molecular genetics - Predictive genetic testing - Targeted panels for inherited (germline) DNA/RNA changes | Blood; Extracted DNA; Tissues | Blood borne tumours; Breast cancer; Hereditary colorectal cancer; Inherited blood borne tumours; Inherited cancer syndromes; Inherited colorectal cancer; Inherited solid tumours; Solid tumours |
| Molecular genetics - RNA extraction | Blood; Buffy coat; Formalin-fixed paraffin-embedded (FFPE) tissues; Tissues | Viable RNA; Viable RNA for sequencing |
| Molecular genetics - Screening for an unknown mutation - Targeted genes | Blood; Extracted DNA; Formalin-fixed paraffin-embedded (FFPE) tissues; Plasma; Tissues | Blood borne tumours; Breast cancer; Inherited blood borne tumours; Inherited cancer syndromes; Inherited solid tumours; Solid tumours |
| Molecular genetics - Screening for an unknown mutation - Targeted panels for non-inherited (somatic) DNA/RNA changes | Blood; Formalin-fixed paraffin-embedded (FFPE) tissues; Fresh tissue | Blood borne tumours; Inherited cancer syndromes; Nucleic acid analysis for unknown variants; Solid tumours |
| Molecular genetics and/or cytogenetics - Bioinformatic analysis | DNA sequences; RNA sequences | Primary analysis - Conversion of instrument file to FASTQ or FASTA file; Tertiary analysis - Data annotation and interpretation |
ISO 15189 (2022)
- This facility complies with the relevant National Pathology Accreditation Advisory Council (NPAAC) requirements.
Human Pathology
| Service | Product | Determinant |
|---|---|---|
| Molecular genetics - Assay for defined mutation or polymorphism (including pharmacogenetic testing) - Targeted genes | Blood; Formalin-fixed paraffin-embedded (FFPE) tissues | Blood borne tumours; Breast cancer; Solid tumours |
| Molecular genetics - DNA extraction | Blood; Formalin-fixed paraffin-embedded (FFPE) tissues | Viable DNA; Viable DNA for sequencing |
| Molecular genetics - Detection and characterisation of cell free RNA (cfRNA) and/or cell free DNA (cfDNA) and/or cell free TNA (cfTNA) and/or circulating tumour DNA (ctDNA) in cancer screening and/or cancer genetic testing | Blood | Nucleic acid analysis for specific variants |
| Molecular genetics - Genetic testing for chimerism and mosaic gene variants (cancer and somatic mosaicism) - Targeted genes | Blood; Formalin-fixed paraffin-embedded (FFPE) tissues | BRCA1 methylation; Blood borne tumours; Inherited cancer syndromes; Nucleic acid analysis for specific variants; Solid tumours |
The only data displayed is that deemed relevant and necessary for the clear description of the activities and services covered by the scope of accreditation.
Grey text appearing in a SoA is additional freetext providing further refinement or information on the data in the preceding line entry.
Accreditation No.
19912
Site No.
23962
Print date
14 Mar 2026