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Next Generation Sequencing
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RNA-SeqProtein Biomarker Detection with OlinkHigh-Throughput Gene Expression Screening NEWSingle-Cell SequencingExome SequencingAmplicon Sequencing ServicesWhole Genome SequencingCRISPR ValidationTargeted SequencingMetagenomicsEpigenomicsAntibody Discovery NEWImmunogenomicsDigital Spatial ProfilingAAV Genome SequencingWhole Plasmid Sequencing: Plasmid-EZ NEW
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Sanger Sequencing
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Sanger-EZ NEWAAV-ITR Sanger SequencingPurified TemplatesDifficult Template SequencingDirect Colony SequencingPCR PurificationPrimer Walking
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PCR + Sanger Services
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Bacterial and Fungal IdentificationMutation AnalysisSNP GenotypingPCR Plus Sequencing CRISPR Analysis PackageConfirmatory Sequencing & Cell Bank CharacterizationYeast Colony SequencingFragment AnalysisQuantitative PCR & Digital PCR NEW
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Gene Synthesis
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Standard Gene Synthesis (PriorityGENE)TurboGENE™Antibody SynthesisAAV Plasmid SynthesisGene FragmentsCRISPR Construct SynthesisssDNA SynthesisDNA CloningSite-Directed Mutagenesis
Viral Packaging NEWRecombinant Antibody Production NEWCustom mRNA Synthesis NEW
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Oligo Synthesis Services
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Overnight DNA OligosCustom DNA and RNA OligosOligo Retained for Sanger Sequencing
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Plasmid DNA Preparation
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Standard Plasmid DNA PrepTargeted Yield Plasmid DNA PrepAAV Plasmid Preparation
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PreClinical and Clinical Services
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Clinical ServicesMicroarray Solutions NEWCLIA Variant Confirmation (PCR + Sanger)CLIA Sanger SequencingCLIA Whole Exome SequencingCLIA Whole Genome SequencingGLP-Compliant OverviewGLP Confirmatory SequencingGLP SNP Mutation AnalysisGLP Plasmid PrepGLP Nucleic Acid ExtractionBiofluid ProcessingCLIA Integration Site Analysis NEW
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10X GENOMICS Chromium™ Controller – NEW!
The 10X GENOMICS Chromium™ Controller enables a diverse set of sequencing applications like whole-genome phasing and structural variant analysis, remapping of difficult regions in the genome, de novo genome assembly, and dynamic gene expression at the single cell level.
Learn more about the instrument here
PacBio® Sequel® System – NEW!
The PacBio® Sequel® System platform is based on PacBio’s proven Single Molecule, Real Time (SMRT®) sequencing technology. This SMRT sequencing on the PacBio Sequel combines long read technology and rapid sequencing with 7 times higher throughput compared to previous systems for the highest-quality data. The PacBio Sequel is ideal for whole genome de novo assembly projects that require higher-quality data, microbial genome assembly, identifying DNA modications without bisulfite treatment, and identifying large structural variants. The system delivers up to 99.999% accuracy. Request a Quote
Learn more about the instrument here
Illumina HiSeq Series
The Illumina® HiSeq™ system is one of the most powerful sequencing machines on the market and is used by most major genome centers and leading institutions around the world. This machine offers ultra-high-throughput sequencing for a myriad of project types. Sequencing is conducted either in the High Output Mode (8 lane flowcell) or Rapid Run Mode (2 lane flowcell). GENEWIZ can accept most projects involving custom indexing and sequencing primers, as well as projects that have different read1 and read2 lengths using the Rapid Run Mode on the HiSeq.
GENEWIZ NGS Platforms and Specifications
GENEWIZ features the most cutting-edge next generation sequencing platforms including the new PacBio Sequel, the powerful Illumina HiSeq X® Ten, Illumina HiSeq, and Illumina MiSeq™. We are a Certified Service Provider (CSPro) for the Illumina sequencing technologies, which guarantees the customer the best data quality.
