Webinars
DNA Genotek's webinar program allows you to find out about various aspects of sample collection and its applications from the comfort of your own desk. Each 60-minute DNA Genotek webinar features an educational discussion, case studies, and a Q&A session.
High Quality Libraries for Human WGS with Direct Saliva Input
Experts in DNA sequencing and DNA from saliva talk about what's trending in whole genome sequencing (WGS). Joshua Burgess, Manager of Research and Development at Illumina, and Rafal Iwasiow, Vice President of Research and Development at DNA Genotek, will discuss why human genomic research is moving towards WGS and what this means for research study design and planning. They will also look at the viability of saliva as a DNA sample source, as compared to blood, for whole genome sequencing using Illumina's Nextera DNA Flex to produce high quality libraries for WGS.
The Key to Eliminating Bias in Genetic Studies Could be in Our Spit
In recent years, saliva has emerged as an increasingly useful source of DNA, making its mark in epigenetic studies of psychiatric diseases, diagnosing HIV, and in the rise of direct-to-consumer genetic testing. The ease of which a saliva sample can be collected and its ability to be stored at room temperature without DNA degradation has allowed for the increased inclusion of children and under-represented, non-European populations in genetic studies. But does the quality and integrity of DNA from saliva match up to the standard? A panel of experts including: Dr. Joan O’Brien, chair of the University of Pennsylvania’s Department of Ophthalmology and Dr. Alicia Smith, Associate Professor and Vice Chair for Research, Gynecology and Obstetrics at Emory University School of Medicine, come together to discuss the benefits and drawbacks on the use of saliva DNA in genetic studies and how it’s currently being used to diminish biases in our databases and uncovering the role of epigenetics in psychiatric disorders.
Microbiome-centric human health: a call for systems biology
Research to date has implicated microbial activity in autoimmune disease, cancer, and the obesity epidemic. As a major source of variability across people, understanding and altering an individual's microbiome is both a challenge and novel avenue for personalized medicine and nutrition. Dr. Eran Segal of the Weizmann Institute of Science, Israel shares his research using OMNIgene·GUT, summarizes the state of the science, and discuss the next steps in developing personalized microbiome-based therapies.
Curating massive amounts of biological material and phenotypic data for robust & reproducible microbiome discovery
Over 100 microbiome-centred therapeutics programs are currently moving through clinical development. Venture and industry investment in the field has topped $1B in the past 5 years. Over that same period, academic research funding has seen compound growth exceeding 20% per year. Of these enormous inputs, what proportion has generated real insight and how much of this output is noise? This short talk will highlight solutions DNA Genotek has deployed for its customers conducting population-scale research and delivering Direct-to-Consumer insights. We make curating massive amounts of biological material and phenotypic information scalable and reproducible.
Integrating the Microbiome into Your Research
Watch this presentation highlighting how you can effectively integrate the microbiome into any genetic research project.
Overcoming Challenges in DNA Sample Acquisition for Cancer Research
Obtaining high quality genomic DNA is critical for studies that aim to evaluate the role of genetic factors in cancer. However, cancer research studies often require very large numbers of samples from a dispersed population and non-invasive methods for DNA collection. Saliva samples, which are painless for the donor and relatively easily collected, are quickly becoming the preferred choice. Cancer research groups around the world are now focusing on the potential of this common bodily fluid for detecting the genetic link to the disease and studying genes.
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