The University of Melbourne, Department of Pathology.
Post author: Tiffany Cowie. Last update: 30/10/2015 at 9:49 am by Tiffany Cowie.
The Melbourne Translational Genomics Platform provides access to a broad range of capabilities, with particular expertise in clinical applications. Our facility offers the following:
- Massively parallel sequencing on the HiSeq2500 and MiSeq
- Sanger sequencing and genotyping
- Custom genetic analysis including established genetic panels for cancer and neurodegenerative disease
- Bioinformatic consultation
- Project design consultation
- NATA accredited molecular and histopathology diagnostic facility
- Specialist expertise in molecular pathology
- NATA accreditation of genomic facility
- Experienced technical and research personnel, internationally recognised in molecular genetics and diagnostics, and the implementation of genomic technology in the clinical setting
Support for experimental design, instrument use and data analysis is available.
Ms. Kym Pham
Ms. Tiffany Cowie
Facility Director at The University of Melbourne, Department of Pathology.
Tiffany Cowie (BSc MBA) is Research Manager for the Centre for Translational Pathology at University of Melbourne.
Former manager and senior scientist of AGD within the Department of Pathology, she also ran the neuroProteomics and neuroGenomics (P&G) Platform of the National Neuroscience Facility and is experienced in operational and strategic management of technology facilities, particularly at the interface of research, clinical practice and commercial service delivery.
P: 03 9035 7914 | Email |
Melbourne Translational Genomics Platform
The University of Melbourne, Department of Pathology. Level 7, Medical Building, Corner Grattan Street and Royal Parade, Parkville, Victoria, Australia.
View location in Google maps.
Type: Core facility in a research organisation
Discipline areas: Biological Science
Affiliations: The University of Melbourne
Accreditation: ISO 17025
Biological Science categories: Bioinformatics, Clinical Trials Design and Managment, Clinical trials resources, Computational, Diagnostics, DNA Sequencing, Expression analysis, Genomics, Genotyping, Methylation analysis, Molecular Profiling, Mutation analysis, Next Generation Sequencing, Preclinical assays