National Association of Testing Authorities, Australia
Scope of Accreditation
Queensland University of Technology
Site
Australian Translational Genomics Centre (ATGC)
Accreditation No.
20179
Site No.
23934
Date of Accreditation
26 Sep 2017
Address
Translational Research Institute, Level 7, 37 Kent Street
Woolloongabba, QLD 4102
Australia
Contact
Mr Sushil Narayan P: +61 (07) 34437280
Availability
Services available to external clients
Supervision
Not Applicable
Scope of Accreditation
Australian Translational Genomics Centre (ATGC)
ISO 15189 (2012)
- This facility complies with the relevant National Pathology Accreditation Advisory Council (NPAAC) requirements.
Human Pathology
Service | Product | Determinant |
---|---|---|
Molecular genetics - DNA extraction | Blood; Saliva; Tissues | Viable DNA for sequencing |
Molecular genetics - DNA sequencing | Blood; Formalin-fixed paraffin-embedded (FFPE) tissues; Hair; Tissues | Incidental germline whole exome sequencing; Sequenced DNA utilising massively parallel sequencing technologies; Somatic whole exome sequencingIncidental Germline findings in a restricted number of genes.es. AIP, ALK, APC, ATM, AXIN2, BAP1, BARD1, BMPR1A, BRCA1, BRAC2, BRIP1, CDC73, |
Molecular genetics - Genetic testing for chimerism and mosaic gene variants (cancer and somatic mosaicism) - Whole exome sequencing for non-inherited (somatic) DNA/RNA changes | Formalin-fixed paraffin-embedded (FFPE) tissues | Solid tumours |
Molecular genetics - RNA extraction | Blood; Saliva; Tissues | Viable RNA for sequencing |
Molecular genetics - RNA sequencing | Extracted RNA | Sequenced RNA utilising massively parallel sequencing technologies |
Molecular genetics - Screening for an unknown mutation - Microarray analysis for inherited (germline) DNA/RNA changes | Blood; Extracted DNA; Saliva | Nucleic acid analysis for unknown variantsWet lab only, No Bioinformatic analysis. |
Molecular genetics - Screening for an unknown mutation - Targeted panels for non-inherited (somatic) DNA/RNA changes | Extracted DNA; Extracted RNA | Nucleic acid analysis for unknown variants |
Molecular genetics - Screening for an unknown mutation - Whole exome sequencing studies for inherited (germline) DNA/RNA changes | Formalin-fixed paraffin-embedded (FFPE) tissues | Inherited solid tumours |
Molecular genetics/Cytogenetics - Bioinformatic analysis | DNA sequences | Primary analysis - Conversion of instrument file to FASTQ or FASTA file; Secondary analysis - Alignment and variant calling; Tertiary analysis - Data annotation and interpretation |
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.
20179
Site No.
23934
Print date
10 Oct 2024
END OF SCOPE