Bioinformatics for Clinical / Health

AGRF provides specialised bioinformatics services to support the clinical and translational research sectors with high-quality, clinically relevant genomic insights. Our expert team works closely with healthcare providers, diagnostic labs, and researchers to deliver accurate, timely, and actionable data interpretations.

We offer customised pipelines and reporting solutions for:

  • Germline and somatic variant analysis

  • Inherited disease and rare disorder diagnostics

  • Oncology and tumour profiling

  • Pharmacogenomics

  • Clinical trial support and biomarker discovery

With a strong focus on data quality, regulatory compliance, and patient relevance, AGRF is a trusted partner in advancing precision medicine and improving health outcomes across Australia.

 
  • Mutations that have been inherited and appear in every cell. 
    Analysis method often used for inherited disease projects.

    Accreditation - ISO15189 (SNVs/InDels) & ISO17025

    Related library preparation methods: WES, WGS, Targeted panels, Illumina Arrays (GSA, GDA), PacBio, Illumina Sequencers

  • Mutations that have been acquired and appear in a subset of cells. Analysis method often used for cancer projects.

    Accreditation - ISO15189 (TSO500) & ISO17025

    Related library preparation methods: WES, WGS, TSO500, Targeted panels

  • Estimating risk of disease using common SNPs

    Related library preparation methods: Illumina Array (GSA, GDA, etc.), WGS

  • Identifying mutations affecting metabolisation of therapeutics

    Related library preparation methods: GDA+ePGx, WGS, Twist Pgx w/ PacBio