The Illumina NovaSeq X Plus brings expanded capacity and new X-LEAP technology to our arsenal of sequencers. These state-of-the art capabilities include unmatched throughput, generating vast amounts of high-quality sequencing data in a single run with ultra-high-resolution imaging across ultra-high-density patterned flow cells. NovaSeq X Plus enables scalability of small-scale studies into genome-wide association studies, generating rapid and actionable results to accelerate your timelines.
In addition to research use only (RUO) services, GENEWIZ Multiomics & Synthesis Solutions from Azenta Life Sciences offer CLIA-validated clinical whole genome and exome sequencing assays and clinical-grade exploratory RUO services on our qualified NovaSeq systems in a CLIA-certified/CAP-accredited laboratory.
The Illumina NovaSeq generates up to 3 trillion bases per run and is optimized to tackle large-scale and deep-sequencing genomics research projects in as fast as one week. As an Illumina provider, GENEWIZ’s optimized workflows deliver superior data, surpassing even Illumina’s own benchmarks. The Illumina S4 flow cell is our most popular option, with 4 sequencing lanes and an output of 2-2.5 billion read pairs (600-750 Gb for 2x150 bp) per lane. Other flow cells and configurations are available upon request.
The Illumina MiSeq is a versatile and cost-effective platform for smaller sequencing projects, including amplicon and microbial genome sequencing. Configurations include 2x150 bp (4.5 Gb for 10-15M read pairs), 2x250 bp (7.5 Gb for 10-15M read pairs), and 2x300 bp (13 Gb for 20-25M read pairs).
The PacBio Revio long-read system expands on HiFi sequencing technology by offering a 15x increase in data throughput compared to previous PacBio platforms, enabling researchers to sequence up to 360 Gb of HiFi reads in a single day. This system features a high-density, 25 million ZMW SMRT® Cell which allows for up to 4 SMRT cells to be run in parallel, achieving 30x HiFi coverage of a human genome with just one SMRT cell.
Long-read lengths (up to 25 kb) and high accuracy (>99.9%) make the Revio ideal for a wide range of genomic applications, including de novo assembly, comprehensive variant detection, single-cell transcriptomics, and epigenetic characterization.
As a PacBio certified service provider, GENEWIZ NGS Solutions help scientists leverage the power of high-throughput sequencing and superior accuracy of long reads to drive genomic analysis beyond what is possible through short-read sequencing.
The PacBio Sequel IIe system is perfect for transcript isoform discovery through PacBio Iso-Seq® and deep sequencing of amplicon libraries. In combination with our team of scientific experts, the Sequel IIe system enables scientists to obtain actionable data faster. PacBio’s HiFi sequencing technology uniquely integrates the benefits of high accuracy with long-read lengths, providing a comprehensive view of genomes and transcriptomes to help scientists tackle complex genetic challenges.
The 10x Genomics Chromium Controller employs microfluidics and molecular barcoding to analyze tens of thousands of individual cells or high-molecular-weight DNA molecules. Applications include single-cell RNA sequencing, single-cell whole genome sequencing, immune V(D)J repertoire profiling, and long-range haplotype phasing. As an early adopter of the Chromium platform, we have developed optimized workflows to maximize project flexibility, speed, and data accuracy.
The 10x Genomics Chromium X Series upgrades single-cell analysis to a scalable and versatile solution using the microfluidics of the first-generation 10x Genomics Chromium Controller. Perform single-cell gene expression, immune profiling, ATAC, Multiome ATAC + Gene Expression, and Flex assays using expanded sample preparation options. In addition to live and frozen cell and tissue types, fixed cell sample types are added allowing for targeted gene expression and multiomic analyses.
As one of three exclusive 10x Global Clinical Research Organizations (CROs), we have adopted the advanced technology of Chromium X to expand the options we provide to our customers.
The NanoString GeoMx Digital Spatial Profiler (DSP), coupled with NanoString’s nCounter® technology, combines morphological and molecular profiling to enable high-resolution analysis of heterogeneous tissue samples. Regions of interest are selected from fluorescently-stained FFPE slides for distinct expression profiling of preconstructed RNA or protein panels. The process is highly quantitative and non-destructive, enabling >100-plex profiling from a single FFPE slide.
By passing DNA or RNA strands through nanopores, Oxford Nanopore Technologies (ONT) can rapidly analyze the electrical signals generated to provide real-time sequence information. This unique approach allows for long-read sequencing for the detection of large structural variations and complex genomic regions, including those with high GC content or repetitive sequences.
The most common application used by our customers is our rapid whole plasmid sequencing service. Contact us for other applications, such as long-read whole genome sequencing and amplicon sequencing.
Olink Proteomics enables high-throughput multiplexed analysis of protein abundance from various biological samples, like serum and plasma. We are proud to offer analysis of over 5,000 proteins on the Olink Explore HT workflow. Additionally, we offer smaller off-the-shelf panels, including Target and Flex, and have also adopted the customized Focus targeted panel.
By coupling our extensive automation capabilities with a fleet of the highest throughput Illumina sequencers, we are equipped to handle projects of any size. All Olink projects are processed in a CLIA-certified/CAP-accredited laboratory, offering further regulation for your important scientific work.