Queensland University of Technology

Site

Australian Translational Genomics Centre (ATGC)

Accreditation No.

20179

Site No.

23934

Date of Accreditation

01 Jun 2017

Address

Translational Research Institute, Level 7, 37 Kent Street
Woolloongabba, QLD 4102
Australia

tri.edu.au/ATGC

Contact

Dr Paul Leo P: +61 0413038691

Availability

Services available to external clients

Supervision

Not Applicable

Queensland University of Technology address map

Scope of Accreditation

Print scopes
Australian Translational Genomics Centre (ATGC)

ISO 15189 (2022)

  • This facility complies with the relevant National Pathology Accreditation Advisory Council (NPAAC) requirements.

Human Pathology

Service Product Determinant

Suspended

Molecular genetics - DNA extraction		 Blood; Saliva; Tissues Viable DNA for sequencing

Suspended

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,

Suspended

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

Suspended

Molecular genetics - RNA extraction		 Blood; Saliva; Tissues Viable RNA for sequencing

Suspended

Molecular genetics - RNA sequencing		 Extracted RNA Sequenced RNA utilising massively parallel sequencing technologies

Suspended

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.

Suspended

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

Suspended

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

Suspended

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.