Illumina NovaSeq™ X Plus

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.

Illumina NovaSeq™ 6000 Sequencing System

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.

In addition to research use only services, GENEWIZ offers CLIA validated clinical whole genome and exome sequencing assays on our CLIA/CAP accredited NovaSeq systems.

Illumina MiSeq™ Series

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).

10x Genomics Chromium™ Controller

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.

10x Genomics Chromium™ X

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.

Oxford Nanopore Platforms

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.