Service & Options
GENEWIZ Sanger sequencing is easy and straight-forward.
GENEWIZ Sanger sequencing is easy and straight-forward.
About GENEWIZ’s Global Network Services GENEWIZ provides a wide range of next generation sequencing services and a broad portfolio of gene synthesis and molecular genetics solutions for research institutions, pharmaceutical companies, and other public, private, and government partners. Through the GENEWIZ Global Network Service (GNS), our customers have access to our state-of the-art laboratories around…
MICROARRAY SOLUTION SERVICES All direct shipments should be sent to: GENEWIZ Attn: Microarrays 111 Corporate Boulevard Suite H Loading Dock South Plainfield, NJ 07080 USA Sample Submission Guidelines Microarray Solutions Back to Top For questions on submitting other, or less than ideal sample types, please contact our Project Management team to discuss…
GENEWIZ standard Gene Synthesis service, PriorityGENE, provides endless opportunities to create any custom sequence for your synthetic biology research.
Bioinformatics Solutions GENEWIZ bioinformatics solutions provide researchers with the tools required to effectively analyze and manage vast quantities of data. Bioinformatics solutions are available as standalone services for bioinformatics projects, as well as in conjunction with our Next Generation Sequencing Services. With flexible and customizable service options, GENEWIZ offers complete and effective solutions for your…
CLIA SANGER-BASED SERVICES All direct shipments should be sent to: GENEWIZ Attn: CLIA Sanger 111 Corporate Boulevard Suite H Loading Dock South Plainfield, NJ 07080 USA Sample Submission Guidelines CLIA Variant Confirmation (PCR + Sanger) Genomic DNA: 60 ng at 20 ng/µl per sample per target is recommended; at least 5 ng at…
CLIA Next Generation Sequencing All direct shipments should be sent to: GENEWIZ Attn: CLIA NGS 111 Corporate Boulevard Suite H Loading Dock South Plainfield, NJ 07080 USA Sample Submission Guidelines DNA Sample Submission Guidelines Whole Exome Sequencing (CLIA-Validated Service) Sample Type: Genomic DNA Recommended Quantity: ≥1 µg Required Quantity: ≥600 ng Concentration: ≥20…
Low-Pass Whole Genome Sequencing (LP-WGS or low-coverage whole-genome sequencing) is an inexpensive high-throughput technology for detecting genome-wide genetic variation in a multitude of species.
GENEWIZ next-generation sequencing based cancer panels provide a complete solution for your cancer research studies from experimental design to advanced bioinformatics analysis.