Pacific Biosciences
Revio
The PacBio Revio system is the latest cutting-edge long-read sequencing platform designed to deliver exceptional accuracy and throughput at scale, meeting the demanding needs of modern research and clinical genomics. Taking advantage of PacBio’s HiFi sequencing technology, the Revio system offers highly accurate long-read sequencing that is ideal for complex genomic analyses, such as de novo genome assembly, detecting rare variants and structural variations, and epigenetic studies.
Generate comprehensive genomic data for everything from microbiome projects to population-scale clinical studies using the scalability and efficiency of the PacBio Revio.
Benefits
- High accuracy
- Long-read capability
- Suitable for complex genomic studies and large-scale projects
Illumina
NovaSeq X+
The NovaSeqX+ is Illumina’s latest high-throughput next generation sequencing (NGS) system that takes advantage of sequencing-by-synthesis and the new X-LEAP chemistry, delivering cost efficient sequencing across a range of project sizes. It is suitable for a range of applications from WGS to transcriptomics, and scales easily with rapid run times. The system delivers high accuracy, high quality data, enabling you to tackle complex research and clinical genomics projects with ease.
Benefits
- Scalability
- Flexibility
- High throughput
- Precision
Illumina
NextSeq 2000
The NextSeq2000 is Illumina’s latest mid-range next generation sequencing (NGS) system that takes advantage of sequencing-by-synthesis and the new X-LEAP chemistry, delivering cost efficient sequencing across a range of project sizes with read lengths from 1 × 50bp to 2 × 300bp . It is suitable for a numerous of applications from WGS to transcriptomics, and scales easily with rapid run times. The system delivers high accuracy, high quality data, enabling you to tackle complex research and clinical genomics projects with ease.
Benefits
- Scalability
- Flexibility
- Mid-range throughput
- Precision
Illumina
iSeq 100
A compact, benchtop NGS system, the Illumina iSeq 100 offers a flexible, cost-effective platform for smaller-scale genomic projects. Taking advantage of Illumina’s sequencing-by-synthesis approach, the iSeq 100 offers high quality data with relative ease. It is well-suited for targeted panels, smaller genomes, and amplicon sequencing, and offers reliable, efficient data at a lower throughput to its NovaSeq counterpart.
Benefits
- Cost-efficient
- Consistent and high-quality sequencing results
Nanostring
nCounter
The Nanostring nCounter platform is a powerful solution for multiplexed gene expression analysis. It offers the ability to quantify up to 800 targets simultaneously, accelerating biomarker validation and development workflows. Compatible with a range of sample types (FFPR, FF, blood, etc.) and requiring minimal sample preparation steps, the nCounter system offers actionable data for oncology, immunology, and neuroscience studies.
Benefits
- High multiplexing capability
- Direct detection of nucleic acids and proteins
- Versatile applications
Oxford Nanopore Technologies
MinION
A compact, portable system, the Oxford Nanopore MinION is a DNA and RNA sequencer with long-read capabilities and real-time data output. It is capable of direct sequencing of RNA, without the need for reverse transcription, and is designed to simplify sample preparation and be cost-effective at the lab bench or in the field. It is particularly suitable for smaller-scale projects that benefit from more immediate data like pathogen detection and environmental monitoring, but is also able to support targeted and whole genome sequencing, metagenomics, transcriptomics, and smaller multiplexing studies.
Benefits
- Real-time data
- Long-read capabilities
- Minimal sample preparation steps
Thermo Fisher Scientific
GeneTitanMC
An automated microarray platform, the Thermo Fisher Scientific GeneTitanMC system is designed for high-throughput genotyping and gene expression analysis. Particularly suited for large-scale studies, it is efficient and minimizes the chance of errors by automating workflow steps from hybridization to imaging. It delivers high resolution data for a range of study types, including genome-wide SNP genotyping, biomarker discovery, and CNV analysis.
Benefits
- Scalability
- Automated workflow for high consistency and data quality
