The publication of the first draft of the human genome in 2001 was a milestone in the genetics field. The following decades saw a dramatic evolution in sequencing strategies and platforms leading to the discovery of some of the most relevant features in our genetic material. Since its foundation, Novogene has been a leader in NGS, with human Whole Genome Sequencing and Whole Exome Sequencing some of our most requested services. In this webinar, you will learn about workflows for both WGS and WES along with bioinformatics analysis options for your data. You will get an overview of different strategies and potential applications suitable for WGS and WES such as biomarker detection, genetic disease studies, cancer research and human population evolution studies, among others.
We are proud to be able to support your research by generating high-quality, publication-ready data in a rapid time-frame. Reach out to us and we will get back to you shortly.
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