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Half-Day Scientific Course (All Levels): Complex Genotype/Phenotype Analysis
Finding links between genetic markers and the end phenotype can be difficult. Apart from drug discovery, combining large cohorts of deeply phenotyped individuals with their genomic data is useful in a wide range of applications, including the development of companion diagnostics, patient stratification, and clinical trial recruitment.

In this All Levels scientific course you’ll learn various scientific applications for detecting the relationship between genotypes and phenotypes. This course will build from Graphical User Interface exercises to more technical Command Line applications.

Agenda: The goal of this half-day course is to expand the skills and knowledge of biomedical researchers and developers. Please join us to learn more about:

-Mutation analysis of WGS data
-‘Slicing and dicing’ cohorts for rapid hypothesis testing (no coding required!)
-Generating clusters of SNPs that are drug responsive
-Validating hypotheses with pre-existing RNAseq analysis Jupyter Notebooks

Registration full? Sign up for our waitlist: https://go.dnanexus.com/l/457982/2020-04-29/7nrxgs

May 19, 2020 10:00 AM in Pacific Time (US and Canada)

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