Learn from the Sanger experts how you can get the most our your DNA Sequencing
his troubleshooting guide is based on common issues seen from samples within GENEWIZ laboratories in the United States.
Discover the value of scRNA-seq in identifying rare cells, characterizing their transcriptomes, and discovering potential biomarkers in this GENEWIZ-exclusive study.
Discover the powerful capability of genoTYPER-NEXT in the illuminating case study, “Rapid, Scalable, and Ultra-Sensitive Validation of Allele-Specific Gene Editing Events.”
Download this tech note now to learn why researchers at a large bio-pharmaceutical company chose GENEWIZ’s Trimer-Controlled Library solution to obtain a highly accurate mutant library.
This study proves the feasibility of multiplexing and highlights the key advantages of the PacBio Sequel platform as compared to its predecessor, the RSII.
This case study looks at how GENEWIZ utilized the PacBio® Sequel™ long-read technology to help a customer improve detection of structural variants within glioblastoma samples.
Learn how to expedite your research by overcoming inefficiencies of traditional approaches while giving you more precise control over sequence diversity.
Discover the benefits of Rolling Circle Amplification (RCA) and how it can save time and hassle by performing direct colony sequencing from bacteria and phage, eliminating plasmid prep.
New technologies are enabling scientific researchers to see results from large whole genome sequencing in a matter of weeks. This piece discusses these new machines and their analysis capabilities.
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