Australia’s Leading Genomics Centre—Right Here in Sydney

High‑throughput sequencing, genotyping & bioinformatics delivered faster and more affordably than overseas labs.

25 years operating

ISO/IEC 17025:2017 accredited

Largest university genomics facility in Australia

Supported by UNSW Sydney

2,000+ project submissions annually

Why Researchers Choose Ramaciotti Centre for Genomics

World‑Class Quality

Illumina NovaSeq X Plus, NextSeq 1000, MiSeq i100 & ONT PromethION 2 solo platforms deliver industry‑leading accuracy. All workflows run under a certified quality management system.

Faster Local Turnaround

Avoid international shipping delays and customs. Receive data in as little as 7 days for standard NGS projects.

Real Cost Savings

Competitive per‑sample pricing—plus zero import duties—keeps your grant dollars where they belong: in your research.

Expert Support, End‑to‑End

Our experienced scientists help you design experiments, perform lab work, and deliver publication‑ready data & bioinformatics.

Services Snapshot

Nanopore Sequencing

Long-read sequencing; structural variation detection; rapid field-based analysis; globally recognised expertise

Accredited workflows

Next generation sequencing & genotyping; ISO/IEC 17025

Need something else? If it involves DNA, RNA, or proteins, we can analyse it.

Category Popular Applications
Whole-Genome Sequencing (WGS) Human, plant, animal, microbial genomes (short and long read)
RNA-Seq & Transcriptomics Total RNA, mRNA, low input, miRNA (short and long read)
Single-Cell RNA Sequencing Microfluidics-free; accessible and affordable
Proteomics Olink Reveal proteomics
Plasmid Sequencing  Fast, affordable turnaround using Sanger and Nanopore for bacterial and synthetic constructs
Nanopore Sequencing Long-read sequencing; structural variation detection; rapid field-based analysis; globally recognised expertise
Amplicon & Metagenomics 16S/18S, ITS, custom panels & shotgun metagenomics
Epigenomics & Methylation WGBS, EM-seq, Infinium EPIC arrays
Client-prepared library sequencing Various options available, fast turnaround time
Accredited workflows Next generation sequencing & genotyping; ISO/IEC 17025 

Success Stories

Researcher testimonial

“The Ramaciotti team’s data quality let us publish in Nature Genetics without additional validation.”
— Dr Amanda Lee, Garvan Institute

Biotech founder testimonial

“Switching from an overseas CRO cut our sequencing costs by 30 % and shaved two weeks off every project.”
— Dr James Nguyen, Biotech Founder

Get a Personalised Quote

Prefer to chat? Call us on +61 2 9385 1241 (Mon–Fri, 9 am–5 pm AEST).

Frequently Asked Questions

  • We can process from single cells to high‑throughput batches; any option is available

  • Absolutely—our project scientists will review your goals and recommend the optimal assay, platform and/or depth.

  • We will provide detailed instructions to maintain sample integrity after acceptance of our quote.

  • Yes—standard deliverables include QC reports, FASTQs/BAMs, and optional differential‑expression or variant‑calling pipelines.