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The Stereo-seq OMNI for FFPE Solution is a groundbreaking spatial transcriptomics platform that enables true single-cell total RNA profiling from challenging FFPE samples. Using an innovative Random Probe design, it delivers precise, species-agnostic RNA capture across continuous tissue areas up to 10 mm × 10 mm. Combining histology with high-resolution gene expression data, Stereo-seq OMNI empowers researchers to explore tissue architecture, host–microorganism interactions, and cellular diversity with unprecedented depth and spatial accuracy.
The Stereo-CITE V1.1 Proteo-Transcriptomics Solution enables simultaneous, in situ analysis of the whole transcriptome and 100+ proteins on the same tissue section with subcellular resolution. By combining CITE-seq with the high-resolution Stereo-seq workflow, it delivers unbiased, spatially resolved maps of RNA and protein expression across centimeter-scale tissue areas. With a streamlined “tissue-to-data” pipeline, Stereo-CITE empowers researchers to decode cell phenotypes, interactions, and tissue architecture—driving new insights into tumor microenvironments, immunotherapy, and drug discovery.
STOmics’ proprietary Stereo-seq™ (SpaTial Enhanced REsolution Omics-sequencing) technology enables researchers to explore the transcriptome with unmatched precision. Delivering subcellular resolution and a broad field-of-view, Stereo-seq allows unbiased whole transcriptome profiling from fresh frozen tissue. With validated compatibility across multiple human, mouse, and other tissue types, it empowers single-cell spatial discovery, improved capture efficiency, and advanced multi-omics integration. Stereo-seq v1.3 offers scalable chip sizes, robust analysis with StereoMap software, and high-definition insights into tissue architecture, cellular interactions, and the tumor microenvironment.
Parse Biosciences offers a suite of scalable single cell sequencing solutions powered by its proprietary Evercode™ combinatorial barcoding technology, enabling researchers to study more cells, more samples, and gain more clarity without the need for expensive instruments. Their Evercode™ Whole Transcriptome provides an end-to-end, instrument-free kit with reagents and intuitive analysis software for large-scale single cell RNA sequencing. Evercode™ Immune Profiling expands these capabilities by pairing TCR αβ or BCR heavy–light chains with whole transcriptome data, allowing sensitive exploration of clonotype diversity and immune responses. For functional genomics, CRISPR Detect brings Evercode’s scalability to pooled CRISPR screens, linking gene perturbations with gene expression at unprecedented depth to power drug discovery, treatment response studies, and pathway mapping. Together, these solutions are transforming single cell research by offering unmatched data quality, exponential scalability, and seamless integration across experiments.
The DNBSEQ-T1+ is one of the fastest T-level benchtop sequencers worldwide, powered by MGI’s advanced DNBSEQ™ technology. With dual flow cell operation, it delivers up to 1.2 Tb of data in just 24 hours, offering unmatched speed and scalability. Designed for flexibility, it supports a wide range of applications—from whole-genome and whole-exome sequencing to oncology, transcriptomics, and microbial studies. The system also features an optional built-in bioinformatics module for automated analysis, streamlining workflows from sequencing to results.
The DNBelab-D4 is a compact digital sample preparation system that integrates all library prep steps into a single fully enclosed cartridge. Using advanced digital microfluidic technology, it performs enzymatic fragmentation, adapter ligation, PCR, purification, quantification, and DNB making with minimal hands-on time (<15 minutes). Designed to prevent cross-contamination, the D4 supports 1–4 samples per run and ensures reliable, high-quality libraries for diverse sequencing applications including WGS, metagenomics, targeted sequencing, and pathogen detection. With portability, automation, and contamination-free operation, DNBelab-D4 streamlines workflows from DNA/RNA input to sequencing-ready libraries.
The DNBSEQ-E25 is an ultra-compact yet powerful sequencer designed for labs that need quick, reliable results without the high costs. Its innovative cartridge-based system makes it incredibly easy to use, maintenance-free, and cost-effective, delivering up to 25 million reads per run. For those looking to streamline their workflows, the E25 can be paired with the DNBelab-D4, an automated library preparation system that simplifies the entire process. With complete walk-away automation, you can prepare your libraries for less than $100 AUD each, making this combination ideal for labs seeking efficient, affordable solutions.
The DNBelab C Series enables efficient, high-throughput preparation of single-cell RNA libraries with scalability and precision. Designed for advanced transcriptomics research, it supports the profiling of thousands of individual cells in parallel, delivering high-quality, reproducible data. With streamlined workflows and compatibility across diverse sequencing platforms, the DNBelab C Series empowers researchers to explore cellular diversity, gene expression dynamics, and complex biological systems at single-cell resolution.
The DNBelab C Series High-throughput Single-cell 5′ RNA & V(D)J Library Preparation Set enables efficient profiling of gene expression alongside TCR/BCR repertoire analysis at single-cell resolution. Used with the DNBelab C-TaiM 4 droplet generator, it streamlines library preparation workflows while ensuring high-quality, reproducible results. Together with the DNBC4Tools analysis package, researchers gain an end-to-end solution for data processing, quality control, and basic analysis—empowering advanced immunology, oncology, and single-cell research.
The MGIEasy Olink Library Circularization Set is designed to streamline the preparation of sequencing-ready libraries for Olink® proteomics data. By enabling efficient library circularization, it ensures compatibility with MGI’s DNBSEQ™ platforms, delivering high-quality, reliable results. With simplified workflows and optimized performance, this kit empowers researchers to unlock deeper insights into protein expression and biomarker discovery through next-generation sequencing.
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