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.
The Illumina HiSeq platforms provide high-throughput sequencing, offering greater flexibility and scalability for a wide variety of project types. HiSeq flow cells contain 8 independent sequencing lanes which can be individually loaded, producing up to 350 million read pairs (106 Gb for 2x150 bp) per lane. GENEWIZ accepts most projects requiring custom indexes and custom sequencing primers.
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).
As the first certified service provider of the PacBio Sequel platform, GENEWIZ scientists possess the necessary experience to get the most out of your samples. With Single Molecule, Real-Time (SMRT®) long-read technology, the PacBio Sequel generates reads up to 100 kb long and gigabases of data per SMRT cell. It is ideal for generating reference quality assemblies of genomes, identifying structural variants, analyzing isoforms (Iso-Seq), and sequencing long amplicons, while delivering up to 99.999% accuracy.
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 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.