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    Copy Number Variation CNV

    Copy Number Variation CNV: is a phenomenon in which divisions of the genome are repeated and the number of repeats in the genome varies between individuals in the human population.

    Webinars

    • JUN 19, 2019 8:00 AM PDT
      C.E. CREDITS
      Exploring the genetic landscape of solid tumors using whole-genome copy number analysis
      JUN 19, 2019 8:00 AM PDT
      Exploring the genetic landscape of solid tumors using whole-genome...
      DATE: June 19, 2019TIME: 8:00am PDT, 11:00am EDT Approximately 80% of all cancers are known to be affected by both somatic mutations and copy number changes. Furthermore, r...
      Speaker: Ravindra Kolhe, MD, PhD , Joanna Przybyl, PhD
      Sponsored By: Thermo Fisher Scientific - Applied Biosystems
      MAY 09, 2019 10:30 AM PDT
      C.E. CREDITS
      Somatic Gene Recombination in the Brain
      MAY 09, 2019 10:30 AM PDT
      Somatic Gene Recombination in the Brain
      Speculations that some form DNA alteration might be utilized by the brain date to the 1960s [1] wherein hypotheses for genomic alterations of germline DNA were proposed for immunoglobulins an...
      Speaker: Jerold Chun, MD, PhD
      Presented at: Genetics & Genomics 2019
      MAY 09, 2017 8:00 AM PDT
      WEBINAR: Deafness in the Genomic Era: Discoveries, Challenges and Opportunities
      MAY 09, 2017 8:00 AM PDT
      WEBINAR: Deafness in the Genomic Era: Discoveries, Challenges...
      DATE: May 9, 2017TIME: 8:00am PT, 11:00am ETHearing loss is the most common sensory defect in humans. It affects 360 million people worldwide and by 2020, that number is predi...
      Speaker: Hela Azaiez, PhD
      Sponsored By: Agilent
      DEC 06, 2016 8:00 AM PST
      Pre-emptive genotyping for pharmacogenomic risk - establishing a benchmark
      DEC 06, 2016 8:00 AM PST
      Pre-emptive genotyping for pharmacogenomic risk - establishing...
      DATE: December 6, 2016 TIME: 8:00am PT, 11:00am ET Adverse drug reactions (ADRs) are one of the leading causes of morbidity and mortality in health care. In the US alone, an est...
      Speaker: Ulrich Broeckel, MD
      Sponsored By: Affymetrix, Affymetrix
      SEP 09, 2015 9:00 AM PDT
      WEBINAR: Clinically actionable gene fusions, CNVs and SNVs detected by NGS-based comprehensive profiling
      SEP 09, 2015 9:00 AM PDT
      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
    JUN 19, 2019 8:00 AM PDT
    C.E. CREDITS
    Exploring the genetic landscape of solid tumors using whole-genome copy number analysis
    JUN 19, 2019 8:00 AM PDT
    Exploring the genetic landscape of solid tumors using whole-genome...
    DATE: June 19, 2019TIME: 8:00am PDT, 11:00am EDT Approximately 80% of all cancers are known to be affected by both somatic mutations and copy number changes. Furthermore, r...
    Speaker: Ravindra Kolhe, MD, PhD , Joanna Przybyl, PhD
    Sponsored By: Thermo Fisher Scientific - Applied Biosystems
    MAY 09, 2019 10:30 AM PDT
    C.E. CREDITS
    Somatic Gene Recombination in the Brain
    MAY 09, 2019 10:30 AM PDT
    Somatic Gene Recombination in the Brain
    Speculations that some form DNA alteration might be utilized by the brain date to the 1960s [1] wherein hypotheses for genomic alterations of germline DNA were proposed for immunoglobulins an...
    Speaker: Jerold Chun, MD, PhD
    Presented at: Genetics & Genomics 2019
    MAY 09, 2017 8:00 AM PDT
    WEBINAR: Deafness in the Genomic Era: Discoveries, Challenges and Opportunities
    MAY 09, 2017 8:00 AM PDT
    WEBINAR: Deafness in the Genomic Era: Discoveries, Challenges...
    DATE: May 9, 2017TIME: 8:00am PT, 11:00am ETHearing loss is the most common sensory defect in humans. It affects 360 million people worldwide and by 2020, that number is predi...
    Speaker: Hela Azaiez, PhD
    Sponsored By: Agilent
    DEC 06, 2016 8:00 AM PST
    Pre-emptive genotyping for pharmacogenomic risk - establishing a benchmark
    DEC 06, 2016 8:00 AM PST
    Pre-emptive genotyping for pharmacogenomic risk - establishing...
    DATE: December 6, 2016 TIME: 8:00am PT, 11:00am ET Adverse drug reactions (ADRs) are one of the leading causes of morbidity and mortality in health care. In the US alone, an est...
    Speaker: Ulrich Broeckel, MD
    Sponsored By: Affymetrix, Affymetrix
    SEP 09, 2015 9:00 AM PDT
    WEBINAR: Clinically actionable gene fusions, CNVs and SNVs detected by NGS-based comprehensive profiling
    SEP 09, 2015 9:00 AM PDT
    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
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