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Uncover the Protein-coding Variants with Cost-effective Human Whole Exome Sequencing
It is estimated that 85% of the disease-causing mutations occur in the exome, a very small fraction (~1%) of the genome. For this reason, exome sequencing provides a cost-effective alternative to whole-genome sequencing. In this webinar, we will go over the hWES project workflow, bioinformatics analysis options, as well as a case study, which will help you to discover how Novogene's services can empower your research. Whether you are conducting studies in rare mendelian disorders, complex disease, cancer research, or human population studies, Novogene’s comprehensive human whole-exome sequencing (hWES) service provides a high-quality, affordable, and convenient solution.

Jun 10, 2020 10:30 AM in Pacific Time (US and Canada)

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