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South Australian Genomics Centre (SAGC) - Flinders Node

FHMRI Platforms Facilities Genomics Facility

The South Australian Genomics Centre (SAGC) was established in July 2020 as a state-wide genomics facility to support research in South Australia, as well as nationally and internationally. 

The SAGC is a partnership between the South Australian Health and Medical Research Institute, University of South Australia, Flinders University, The University of Adelaide, the Australian Genome Research Facility (AGRF), and the Australian Wine Research Institute (AWRI). Its establishment was supported by an investment of >$7 million, including $2 million from BioPlatforms Australia (BPA).

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SAGC Services 

Equipment 

Contact Flinders Node 

SA Genomics website

The vision of the SAGC is to enable innovative genomics research by providing state-of-the-art, collaborative end-to-end genomics and bioinformatics services, know-how, and cutting-edge infrastructure.

Services

The SAGC provides a broad range of services including single cell and spatial transcriptomics, RNA sequencing, whole exome and genome sequencing, epigenomics, metagenomics and a range of other custom methods. These services are supported by a dedicated Bioinformatics Platform that supports users of the facility by developing advanced and customised approaches for data analysis, integration and visualisation. All areas of genomics including animal, plant, environmental, microbial, and human genomics are supported.

The South Australian Genomics Centre (SAGC) provides a broad range of services including:

  • Spatial Transcriptomics
  • Single Cell Sequencing
  • Whole genome
  • Whole Exome and Targeted Panels
  • Epigenome
  • Microbiome and Custom Target
  • RNA Sequencing
  • Next generation sequencing

SAGC Services

Equipment

NGS Platforms keyboard_arrow_up

The SAGC offers both Illumina and MGI sequencing. We offer a range of next generation sequencing platforms to find an efficient match for projects of any size. See our range of next generation sequencers with available flow cells and output.

Stereo-seq (STOmics) – MGI keyboard_arrow_up

STOmics (SpaTial Enhanced Resolution Omics-Sequencing): whole transcriptomics for discovery applications (range of 1000-2000 genes/cell) leverages in situ mRNA capture and cDNA sequencing with barcoded spatial coordinates to create a spatial transcriptomic profile of the tissue section for analysis.

  • Subcellular spatial localization of mRNA
  • Chip design ~320M spatially barcoded spots/cm2
  • Spot size = 200 nm diameter
  • Range of field size to accommodate larger tissue samples (up to 13 cm x 13cm)
Xenium in situ Analyser - 10X Genomics keyboard_arrow_up

Xenium Analyser allows targeted gene expression and protein quantification at subcellular resolution. Xenium is an end-to-end platform that enables high-throughput subcellular mapping of RNA targets.

  • Menu of off-the-shelf gene panels + order 100 custom add-on genes
  • Compatible with fresh frozen (FF) and formalin-fixed, paraffin-embedded (FFPE) tissues
  • Microscopy based read-out (no NGS), allows H&E post-run
  • Single molecule RNA and Protein targets (subcellular resolution)
VisiumHD Spatial Transcriptomics - 10X Genomics keyboard_arrow_up

VisiumHD Spatial Transcriptomics allows whole transcriptome mapping within morphological context of complex tissue samples. There is no need to select targets or specific region of interest. Compatible with FFPE and is CytAssist enabled which allows transfer of archived tissue slides to the special barcoded Visium slides to both improve workflow and reduce RNA diffusion.

Chromium Single Cell - 10X Genomics keyboard_arrow_up

Genomics SAGC has a Chromium Controller and Chromium X Series from 10X Genomics to enable multiomic analysis through droplet GEM-based single cell partitioning and sequencing.

Applications available:

  • Single cell RNA expression
  • Single cell Immune Profiling
  • Single cell ATAC
  • Single cell ATAC + RNA expression
  • Single cell RNA expression Flex (FFPE)

*Cell surface marker tagging can be incorporated into some of these techniques and quantified during sequencing.

Compatible with fixed, fresh, and frozen samples, as well as whole cells and nuclei.

Evercode Single Cell – Parse Biosciences keyboard_arrow_up

Evercode is a plate-based combinatorial barcoding technology that enables very large single cell experiments (up to 1 M cells or 96 samples) in a single workflow with either fixed or fresh cells. This approach can offer some advantages with certain cell types and achieve higher throughput at a lower cost compared to microfluidic based approaches.

Contact us

SAGC Flinders Node Facility Manager: Benjamin.Mayne@sahmri.com

Bioinformatics: Daniel.Thomson@sahmri.com

Contact SAGC

+61 8 8204 5446

Visit us

The SAGC Flinders Node is located at the Flinders Centre for Innovation in Cancer (FCIC) at Flinders Medical Centre, Flinders Drive, Bedford Park SA 5042 (Room 4L160)

The SAGC central hub is located in the SAHMRI building (North Terrace, Adelaide, SA). 

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Sturt Rd, Bedford Park
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Last Updated: 22 Jul 2024

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