High-throughput genotyping is a next generation sequencing (NGS) assay ideal for ultra-sensitive, high-throughput, sample-to-answer genotyping projects, enabling validation of targeted CRISPR gene editing experiments.
Whole genome sequencing (WGS) is the comprehensive read and analysis of an entire genome, including non-coding regions of the genome.
GENEWIZ offers standalone next generation sequencing solutions for researchers who are equipped to perform NGS in their own labs but wish to outsource portions of their NGS workflow.
Amplicon sequencing is a targeted sequencing method that uses polymerase chain reaction (PCR) to selectively amplify specific DNA fragments or genomic regions of interest.
Whole exome sequencing is a powerful tool to investigate genetic variations underlying cancers, Mendelian diseases, and complex human disorders.
Single-cell sequencing provides transcriptional profiling of thousands of individual cells.
High-throughput gene expression (HT-GEx) screening is an optimal approach for drug discovery and analysis, similar to DRUG-Seq.
View GENEWIZ case studies and webinars to understand the latest developments in next generation sequencing and gene synthesis technologies.
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