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    Genotyping

    Genotyping: the process of determining differences in the genetic make-up (genotype) of an individual by examining the individual's DNA sequence using biological assays and comparing it to another individual's sequence or a reference sequence. It reveals the alleles an individual has inherited from their parents. Traditionally genotyping is the use of DNA sequences to define biological populations by use of molecular tools. It does not usually involve defining the genes of an individual.

    Webinars

    • FEB 24, 2016 | 8:00 AM
      Keynote Presentation - Integrating the digital universe of data with consumer-driven mobile apps and large-scale panomics data to better understand, treat, and prevent disease
      Keynote Presentation - Integrating the digital universe of data...
      One of the primary goals of precision medicine is the aggregation and interpretation of deep, longitudinal patient-specific data in the context of the digital universe of information, using a...
      Speaker: Eric Schadt, PhD
      Presented at: Precision Medicine Virtual Event Series 2016
      2
      FEB 24, 2016 | 7:00 AM
      Towards precision medicine
      Towards precision medicine
      Understanding disease at a deeper level so that it can be targeted more precisely is the essence of precision medicine. Rapid technological advance, particularly in genomics and sensor-based...
      Speaker: Euan Ashley, MRCP, DPhil
      Presented at: Precision Medicine Virtual Event Series 2016
      2
      FEB 24, 2016 | 7:00 AM
      Precision Medicine Approaches and the Future of Drug Development in Oncology
      Precision Medicine Approaches and the Future of Drug Development...
      A number of recently publications have heralded the advent of Precision Medicine in Oncology, where next generation sequencing technology, other ’omics technologies, serial biopsies, so...
      Speaker: Thomas Metcalfe
      Presented at: Precision Medicine Virtual Event Series 2016
      3
      FEB 24, 2016 | 6:00 AM
      Emerging role of liquid biopsies and NGS for biomarker discovery
      Emerging role of liquid biopsies and NGS for biomarker discovery
      Precision medicine promises a more effective approach to disease treatment and management. It is based on analyzing mutations of disease samples to unlock mechanisms of disease development an...
      Speaker: Raed Samara, PhD
      Presented at: Precision Medicine Virtual Event Series 2016
      2
      FEB 24, 2016 | 6:00 AM
      The 100,000 genomes project
      The 100,000 genomes project
      In December 2012 the UK Prime Minister announced the 100,000 genomes project to introduce whole genome sequencing for treatment into the UK National Health Service (NHS) o...
      Speaker: Tim Hubbard, PhD
      Presented at: Precision Medicine Virtual Event Series 2016
      4
      FEB 24, 2016 | 5:00 AM
      How Personalised Healthcare is transforming drug development
      How Personalised Healthcare is transforming drug development
      Personalised Healthcare is essential to AstraZeneca’s approach to drug development and is adopted by more than 80% of drug products in clinical development. Selection of the right patie...
      Speaker: Ruth March, PhD
      Presented at: Precision Medicine Virtual Event Series 2016
      2
      SEP 09, 2015 | 9:00 AM
      WEBINAR: Clinically actionable gene fusions, CNVs and SNVs detected by NGS-based comprehensive profiling
      WEBINAR: Clinically actionable gene fusions, CNVs and SNVs detected...
      DATE: September 9, 2015TIME: 9:00am PDT, 12:00PM EDTDriver mutations are causally implicated in tumorigenesis and disease progression, and they are defined by molecular abnormalities such as ...
      Speaker: A. John Iafrate, MD, PhD
      Sponsored By: Archer DX, Archer DX
      7 1
      MAY 14, 2015 | 1:30 PM
      Epigenomic Profiles of Asthma
      Epigenomic Profiles of Asthma
      Asthma is heritable, influenced by the environment, and is modified by in utero exposures and aging; all of these features are also common to epigenetic regulation. Furthermore, genetic varia...
      Speaker: Ivana Yang, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2015
      2
      MAY 14, 2015 | 7:30 AM
      Keynote: Using genomics to understand human health and disease
      Keynote: Using genomics to understand human health and disease
      I will discuss the use of genomic technologies - mostly ultrahigh-throughput DNA sequencing - to study normal human biology and to determine what goes wrong when we have disease. First I wil...
      Speaker: Richard Myers, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2015
      6
      MAY 13, 2015 | 3:00 PM
      Using the network architecture of eQTLs to understand complex traits
      Using the network architecture of eQTLs to understand complex...
      Genome Wide Association Studies (GWAS) and eQTL analyses are producing huge numbers of associations and show no signs of slowing. There are now more than 8,500 SNPs associated with more than...
      Speaker: John Platig, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2015
      2
      MAY 13, 2015 | 10:30 AM
      Population Scale Human Genome Analysis on the Cloud
      Population Scale Human Genome Analysis on the Cloud
      Advanced sequencing technologies have made population scale whole genome sequencing a possibility. However, current strategies for analysis of this data rely upon parallelization approaches t...
      Speaker: Peter White, PhD, James Hirmas
      Presented at: Genetics and Genomics Virtual Event Series 2015
      4
      MAR 18, 2015 | 3:00 PM
      The Human Connectome Project
      The Human Connectome Project
      Recent advances in noninvasive neuroimaging have set the stage for the systematic exploration of human brain circuits in health and disease. The Human Connectome Project (HCP) is systematical...
      Speaker: David Van Essen, PhD
      Presented at: Neuroscience Virtual Event Series 2015
      10
      AUG 21, 2014 | 9:45 AM
      Pathway based analyses for genetic susceptibility to cancer and autoimmune disease
      Pathway based analyses for genetic susceptibility to cancer and...
      In this presentation I describe pathway based analyses of genotyping data to identify pathways related to the development of complex diseases, with a focus on lung cancer and selected autoimm...
      Speaker: Christopher I Amos, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2014
      62
      AUG 20, 2014 | 8:45 AM
      Novel gene chip technologies and NGS sequencing for personalized medicine & diagnostic
      Novel gene chip technologies and NGS sequencing for personalized...
      The flexibility of the BioMark Real-Time PCR System, allow us to preform genetic research using different types of nano-fluidic (48.48 or 96.96) chips setup, in the thermal cycle of these chi...
      Speaker: Dani Bercovich, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2014
      12
      NOV 20, 2013 | 8:00 AM
      A comparison of genotyping platforms for pharmacogenetic testing
      A comparison of genotyping platforms for pharmacogenetic testing
      As the scientific evidence base for pharmacogenetics continues to expand, the use of such information in clinical management and drug development will be in demand. The FDA advises that the...
      Speaker: Mark Borgman, PhD
      Presented at: Advanced Genomics in Clinical and Translational Research - Fall
      210
      AUG 21, 2013 | 8:00 AM
      Post Genome-Wide Association Studies
      Post Genome-Wide Association Studies
      In this presentation I describe some of the approaches we are taking to identify the genetic architecture of common complex cancers with a particular focus on the etiology of lung cancer. Can...
      Speaker: Christopher I Amos, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2013
      105
      MAY 30, 2013 | 12:00 PM
      Companion Diagnostics Co-Development: Are you ready?
      Companion Diagnostics Co-Development: Are you ready?
      Development of a companion diagnostic can be critical to the success of a drug. Pharmaceutical companies are committing more and more of their efforts to discover and deliver targeted therapi...
      Speaker: Janice Au-Young, PhD
      Presented at: Clinical Diagnostics Virtual Event Series 2013
      15
    FEB 24, 2016 | 8:00 AM
    Keynote Presentation - Integrating the digital universe of data with consumer-driven mobile apps and large-scale panomics data to better understand, treat, and prevent disease
    Keynote Presentation - Integrating the digital universe of data...
    One of the primary goals of precision medicine is the aggregation and interpretation of deep, longitudinal patient-specific data in the context of the digital universe of information, using a...
    Speaker: Eric Schadt, PhD
    Presented at: Precision Medicine Virtual Event Series 2016
    2
    FEB 24, 2016 | 7:00 AM
    Towards precision medicine
    Towards precision medicine
    Understanding disease at a deeper level so that it can be targeted more precisely is the essence of precision medicine. Rapid technological advance, particularly in genomics and sensor-based...
    Speaker: Euan Ashley, MRCP, DPhil
    Presented at: Precision Medicine Virtual Event Series 2016
    2
    FEB 24, 2016 | 7:00 AM
    Precision Medicine Approaches and the Future of Drug Development in Oncology
    Precision Medicine Approaches and the Future of Drug Development...
    A number of recently publications have heralded the advent of Precision Medicine in Oncology, where next generation sequencing technology, other ’omics technologies, serial biopsies, so...
    Speaker: Thomas Metcalfe
    Presented at: Precision Medicine Virtual Event Series 2016
    3
    FEB 24, 2016 | 6:00 AM
    Emerging role of liquid biopsies and NGS for biomarker discovery
    Emerging role of liquid biopsies and NGS for biomarker discovery
    Precision medicine promises a more effective approach to disease treatment and management. It is based on analyzing mutations of disease samples to unlock mechanisms of disease development an...
    Speaker: Raed Samara, PhD
    Presented at: Precision Medicine Virtual Event Series 2016
    2
    FEB 24, 2016 | 6:00 AM
    The 100,000 genomes project
    The 100,000 genomes project
    In December 2012 the UK Prime Minister announced the 100,000 genomes project to introduce whole genome sequencing for treatment into the UK National Health Service (NHS) o...
    Speaker: Tim Hubbard, PhD
    Presented at: Precision Medicine Virtual Event Series 2016
    4
     
     
  • FEB 24, 2016 | 5:00 AM
    How Personalised Healthcare is transforming drug development
    How Personalised Healthcare is transforming drug development
    Personalised Healthcare is essential to AstraZeneca’s approach to drug development and is adopted by more than 80% of drug products in clinical development. Selection of the right patie...
    Speaker: Ruth March, PhD
    Presented at: Precision Medicine Virtual Event Series 2016
    2
    SEP 09, 2015 | 9:00 AM
    WEBINAR: Clinically actionable gene fusions, CNVs and SNVs detected by NGS-based comprehensive profiling
    WEBINAR: Clinically actionable gene fusions, CNVs and SNVs detected...
    DATE: September 9, 2015TIME: 9:00am PDT, 12:00PM EDTDriver mutations are causally implicated in tumorigenesis and disease progression, and they are defined by molecular abnormalities such as ...
    Speaker: A. John Iafrate, MD, PhD
    Sponsored By: Archer DX, Archer DX
    7 1
    MAY 14, 2015 | 1:30 PM
    Epigenomic Profiles of Asthma
    Epigenomic Profiles of Asthma
    Asthma is heritable, influenced by the environment, and is modified by in utero exposures and aging; all of these features are also common to epigenetic regulation. Furthermore, genetic varia...
    Speaker: Ivana Yang, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2015
    2
    MAY 14, 2015 | 7:30 AM
    Keynote: Using genomics to understand human health and disease
    Keynote: Using genomics to understand human health and disease
    I will discuss the use of genomic technologies - mostly ultrahigh-throughput DNA sequencing - to study normal human biology and to determine what goes wrong when we have disease. First I wil...
    Speaker: Richard Myers, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2015
    6
    MAY 13, 2015 | 3:00 PM
    Using the network architecture of eQTLs to understand complex traits
    Using the network architecture of eQTLs to understand complex...
    Genome Wide Association Studies (GWAS) and eQTL analyses are producing huge numbers of associations and show no signs of slowing. There are now more than 8,500 SNPs associated with more than...
    Speaker: John Platig, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2015
    2
     
     
  • MAY 13, 2015 | 10:30 AM
    Population Scale Human Genome Analysis on the Cloud
    Population Scale Human Genome Analysis on the Cloud
    Advanced sequencing technologies have made population scale whole genome sequencing a possibility. However, current strategies for analysis of this data rely upon parallelization approaches t...
    Speaker: Peter White, PhD, James Hirmas
    Presented at: Genetics and Genomics Virtual Event Series 2015
    4
    MAR 18, 2015 | 3:00 PM
    The Human Connectome Project
    The Human Connectome Project
    Recent advances in noninvasive neuroimaging have set the stage for the systematic exploration of human brain circuits in health and disease. The Human Connectome Project (HCP) is systematical...
    Speaker: David Van Essen, PhD
    Presented at: Neuroscience Virtual Event Series 2015
    10
    AUG 21, 2014 | 9:45 AM
    Pathway based analyses for genetic susceptibility to cancer and autoimmune disease
    Pathway based analyses for genetic susceptibility to cancer and...
    In this presentation I describe pathway based analyses of genotyping data to identify pathways related to the development of complex diseases, with a focus on lung cancer and selected autoimm...
    Speaker: Christopher I Amos, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2014
    62
    AUG 20, 2014 | 8:45 AM
    Novel gene chip technologies and NGS sequencing for personalized medicine & diagnostic
    Novel gene chip technologies and NGS sequencing for personalized...
    The flexibility of the BioMark Real-Time PCR System, allow us to preform genetic research using different types of nano-fluidic (48.48 or 96.96) chips setup, in the thermal cycle of these chi...
    Speaker: Dani Bercovich, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2014
    12
    NOV 20, 2013 | 8:00 AM
    A comparison of genotyping platforms for pharmacogenetic testing
    A comparison of genotyping platforms for pharmacogenetic testing
    As the scientific evidence base for pharmacogenetics continues to expand, the use of such information in clinical management and drug development will be in demand. The FDA advises that the...
    Speaker: Mark Borgman, PhD
    Presented at: Advanced Genomics in Clinical and Translational Research - Fall
    210
     
     
  • AUG 21, 2013 | 8:00 AM
    Post Genome-Wide Association Studies
    Post Genome-Wide Association Studies
    In this presentation I describe some of the approaches we are taking to identify the genetic architecture of common complex cancers with a particular focus on the etiology of lung cancer. Can...
    Speaker: Christopher I Amos, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2013
    105
    MAY 30, 2013 | 12:00 PM
    Companion Diagnostics Co-Development: Are you ready?
    Companion Diagnostics Co-Development: Are you ready?
    Development of a companion diagnostic can be critical to the success of a drug. Pharmaceutical companies are committing more and more of their efforts to discover and deliver targeted therapi...
    Speaker: Janice Au-Young, PhD
    Presented at: Clinical Diagnostics Virtual Event Series 2013
    15
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