Learn from the Sanger experts how you can get the most our your DNA Sequencing
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.
Variant Synthesis can 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.
Learn more about research-level and GLP-compliant mutation analysis and SNP (single nucleotide polymorphisms) discovery. Includes a comparison of in-house mutation analysis and GENEWIZ’s services.
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