AGRF offers high-throughput, cost-effective Illumina BeadChip genotyping for both human and non-human samples. This platform enables whole genome or targeted genotyping to detect common variants and copy number variants (CNVs)—supporting a wide range of applications, including:

• Genome-Wide Association Studies (GWAS)

• Precision medicine pharmacogenomics

• Cytogenetics

• Translational research

• Disease association studies

The Illumina Infinium Global Screening Array (GSA v3) is one of AGRFs most widely used genotyping array. It provides flexible and affordable solutions for research and clinical applications, curated for global populations, the GSA can also be customised to include additional content relevant to your study through a range of booster content options. Take a look at available booster content.

The Illumina Infinium Global Diversity Array (GDA) offers enhanced genome-wide coverage and increased representation of diverse global populations, making it an excellent choice for population-scale studies and translational research. Like the GSA, the GDA can be tailored with booster content—allowing the addition of disease-specific, pharmacogenomic, or trait-focused markers to suit your project needs. Learn more.

AGRF now also offers Polygenic Risk Scores (PRS) powered by Allelica, providing insights into individual genetic risk across a range of complex diseases—an excellent companion to GSA or GDA-based genotyping for researchers.

AGRF supports genotyping of non-human species, with a range of species-specific and consortium arrays available for livestock, companion animals, crops, and more.

To find the best array for your study, contact our team for tailored support, or use our ‘Find my SNP’ tool to explore SNPs present on the range of Illumina arrays.

AGRF now also offers Polygenic Risk Scores (PRS) powered by Allelica, providing insights into individual genetic risk across a range of complex diseases—an excellent companion to GSA-based genotyping for researchers.

AGRF offers Genotyping by Sequencing using the double-digest Restriction-site Associated DNA (ddRAD) protocol—an efficient, scalable approach for SNP discovery and genotyping across a wide range of species.

This method is ideal for both model and non-model organisms, reducing genome complexity while enabling high-throughput and highly multiplexed sequencing.

Our validated ddRAD workflow delivers robust, cost-effective genotyping—especially valuable when working with species that lack a reference genome.

A highly flexible and accurate platform for low- to mid-plex genotyping. Ideal for targeted SNP panels, somatic mutation detection, and validation of NGS findings. The MassARRAY system offers quick turnaround and cost-effective analysis with high specificity and sensitivity.

For an overview of our custom genotyping service, take a look at our service guide.

AGRF provides flexible Custom Microsatellite Genotyping services for a wide range of species. Our team can assist with the design or optimisation of panels using published markers or existing primers.

We offer:

• Support with project and primer design

• Multi-loading strategies to improve efficiency and reduce cost

• High-sensitivity detection using fluorescent PCR and capillary electrophoresis on the 3730 platform

This service is ideal for applications such as population genetics, parentage testing and breeding program support.

AGRF offers fragment analysis using fluorescent capillary electrophoresis on the 3730 platform, supporting a range of applications. These workflows are based on client-supplied PCR products and can be provided as electrophoresis-only or include both electrophoresis and analysis, depending on project needs.

Our services include:

• Microsatellite (Short Tandem Repeat [STR]) Genotyping

• T-RFLP (Terminal Restriction Fragment Length Polymorphisms)

• MLPA (Multiplex Ligation-dependent Probe Amplification)

• AFLP (Amplified Fragment Length Polymorphism)

AGRF’s capillary electrophoresis services are high-throughput, cost-effective, and supported by expert staff to ensure reliable and reproducible results.

AGRF offers NGS services for the discovery of genetic variation in both model and non-model organisms.

We support:

• SNP discovery for population genetics and trait association

• Microsatellite discovery for parentage, diversity, and conservation studies

Our end-to-end service includes sequencing and bioinformatics, tailored to your project needs.

Get in touch to discuss the best approach for your research.

AGRF offers a suite of DNA-based identification services to verify species, confirm sample identity, and detect contamination across a wide range of research and industry needs.

Our services include:

• Human Cell Line Authentication – Confirm the identity and purity of human cell lines to prevent cross-contamination and ensure data integrity.

• Human Exome ID – Identify human samples based on exome-level variation for traceability and sample tracking.

• Human DNA Contamination Screening – Detect trace levels of human DNA in non-human samples, supporting clinical, microbial, and forensic workflows.

• Mouse Linkage Marker Set – Genotype mice using a validated panel of markers for strain verification and linkage analysis.

AGRF is your trusted partner in world class clinical genomics, delivering high quality insights
to genetically inherited conditions.

Providing screening
for three of the most common inherited genetic diseases impacting Australian children.

CFTR - Cystic Fybrosis (CF)
SMN1 - Spinal Muscular Atrophy
FMR1 - Fragile X Syndrome

Click here for more information on Carrier Screening Assays.