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

tri.edu.au/ATGC

Contact

Mr Sushil Narayan P: +61 (07) 34437280

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 (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.