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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

    • MAR 20, 2024 | 8:00 AM
      Deciphering Tissue Complexity: Comprehensive Multi-omic Profiling with the SH800 Cell Sorter and ResolveOMEâ„¢ Amplification
      Deciphering Tissue Complexity: Comprehensive Multi-omic Profiling...
      Deciphering somatic mosaicism in healthy tissues and clonal diversity in tumors necessitates single-cell analysis. High-quality genomic and transcriptomic data at the single-cell level depen...
      Speaker: Jon Zawistowski, Ph.D.
      Sponsored By: Sony Biotechnology
      10
      APR 19, 2022 | 5:30 AM
      Scalable Pharmacogenetic Screening of the Complex CYP2D6 Locus Using SMRT Long-read Amplicon Sequencing
      Scalable Pharmacogenetic Screening of the Complex CYP2D6 Locus...
      The CYP2D6 enzyme metabolizes approximately 25% of commonly used pharmaceuticals and is of intense pharmacogenetic interest. Polymorphisms in CYP2D6 can alter an individual’s response...
      Speaker: Jacob Munro
      Presented at: Genetics Week Virtual Event Series 2022
      1
      FEB 09, 2022 | 9:00 AM
      An Approach to Ultrasensitive Detection and Quantification of Copy Number Variations (CNVs) and Mutations
      An Approach to Ultrasensitive Detection and Quantification of...
      Date: February 09, 2021 Time: 09:00am (PST), 12:00pm (EST) In this webinar we introduce quantitative amplicon sequencing (QASeq): a highly-sensitive and robust NGS-based method for the detec...
      Speaker: Nicolas Garreau de Loubresse, Ph.D. , Jinny Zhang, Ph.D.
      Sponsored By: Nuprobe
      20
      OCT 22, 2020 | 1:15 PM
      Utilizing the Genexus System to Detect Complex Genetic Variants in Human Tissue Specimens
      Utilizing the Genexus System to Detect Complex Genetic Variants...
      To identify genetic variants in archival human samples, researchers need a powerful NGS platform that can accommodate input DNA and RNA that is often low quality and/or low quantity. This ch...
      Speaker: Craig Mackinnon, MD, PhD
      Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
      0
      OCT 22, 2020 | 7:40 AM
      First Experiences with Oncomineâ„¢ Comprehensive Assay Plus for comprehensive genomic profiling
      First Experiences with Oncomineâ„¢ Comprehensive Assay Plus for...
      Identification of actionable mutations, determination of tumor mutational burden (TMB) and microsatellite (MS) status are paramount to precision oncology and the Oncomine Comprehensive Assay...
      Speaker: Ines Raineri, MD
      Presented at: OncomineWorld Autumn: A virtual NGS education meeting
      1
      OCT 22, 2020 | 7:40 AM
      First Experiences with Oncomineâ„¢ Comprehensive Assay Plus for comprehensive genomic profiling
      First Experiences with Oncomineâ„¢ Comprehensive Assay Plus for...
      IIdentification of relevant mutations, determination of tumor mutational burden (TMB) and microsatellite (MS) status are paramount to precision oncology research and the Oncomine Comprehensi...
      Speaker: Ines Raineri, MD
      Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
      0
      JUL 02, 2020 | 2:00 PM
      Applications of CytoMicroarrays
      Applications of CytoMicroarrays
      Genomic imbalances or copy number variations (CNVs) are a major cause of pregnancy losses, fetal anomalies identified during prenatal period, congenital defects in newborn, dysmorphology and...
      Speaker: Anuradha Udumudi, PhD
      Presented at: APJ Virtual Genetic Solutions Tour 2020
      2
      JUN 19, 2019 | 8:00 AM
      Exploring the genetic landscape of solid tumors using whole-genome copy number analysis
      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
      4
      MAY 09, 2019 | 10:30 AM
      Somatic Gene Recombination in the Brain
      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 and Genomics Virtual Event Series 2019
      2
      MAY 09, 2017 | 8:00 AM
      WEBINAR: Deafness in the Genomic Era: Discoveries, Challenges and Opportunities
      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
      11 8
      DEC 06, 2016 | 8:00 AM
      Pre-emptive genotyping for pharmacogenomic risk - establishing a benchmark
      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
      6
      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
    MAR 20, 2024 | 8:00 AM
    Deciphering Tissue Complexity: Comprehensive Multi-omic Profiling with the SH800 Cell Sorter and ResolveOMEâ„¢ Amplification
    Deciphering Tissue Complexity: Comprehensive Multi-omic Profiling...
    Deciphering somatic mosaicism in healthy tissues and clonal diversity in tumors necessitates single-cell analysis. High-quality genomic and transcriptomic data at the single-cell level depen...
    Speaker: Jon Zawistowski, Ph.D.
    Sponsored By: Sony Biotechnology
    10
    APR 19, 2022 | 5:30 AM
    Scalable Pharmacogenetic Screening of the Complex CYP2D6 Locus Using SMRT Long-read Amplicon Sequencing
    Scalable Pharmacogenetic Screening of the Complex CYP2D6 Locus...
    The CYP2D6 enzyme metabolizes approximately 25% of commonly used pharmaceuticals and is of intense pharmacogenetic interest. Polymorphisms in CYP2D6 can alter an individual’s response...
    Speaker: Jacob Munro
    Presented at: Genetics Week Virtual Event Series 2022
    1
    FEB 09, 2022 | 9:00 AM
    An Approach to Ultrasensitive Detection and Quantification of Copy Number Variations (CNVs) and Mutations
    An Approach to Ultrasensitive Detection and Quantification of...
    Date: February 09, 2021 Time: 09:00am (PST), 12:00pm (EST) In this webinar we introduce quantitative amplicon sequencing (QASeq): a highly-sensitive and robust NGS-based method for the detec...
    Speaker: Nicolas Garreau de Loubresse, Ph.D. , Jinny Zhang, Ph.D.
    Sponsored By: Nuprobe
    20
    OCT 22, 2020 | 1:15 PM
    Utilizing the Genexus System to Detect Complex Genetic Variants in Human Tissue Specimens
    Utilizing the Genexus System to Detect Complex Genetic Variants...
    To identify genetic variants in archival human samples, researchers need a powerful NGS platform that can accommodate input DNA and RNA that is often low quality and/or low quantity. This ch...
    Speaker: Craig Mackinnon, MD, PhD
    Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
    0
    OCT 22, 2020 | 7:40 AM
    First Experiences with Oncomineâ„¢ Comprehensive Assay Plus for comprehensive genomic profiling
    First Experiences with Oncomineâ„¢ Comprehensive Assay Plus for...
    Identification of actionable mutations, determination of tumor mutational burden (TMB) and microsatellite (MS) status are paramount to precision oncology and the Oncomine Comprehensive Assay...
    Speaker: Ines Raineri, MD
    Presented at: OncomineWorld Autumn: A virtual NGS education meeting
    1
     
     
  • OCT 22, 2020 | 7:40 AM
    First Experiences with Oncomineâ„¢ Comprehensive Assay Plus for comprehensive genomic profiling
    First Experiences with Oncomineâ„¢ Comprehensive Assay Plus for...
    IIdentification of relevant mutations, determination of tumor mutational burden (TMB) and microsatellite (MS) status are paramount to precision oncology research and the Oncomine Comprehensi...
    Speaker: Ines Raineri, MD
    Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
    0
    JUL 02, 2020 | 2:00 PM
    Applications of CytoMicroarrays
    Applications of CytoMicroarrays
    Genomic imbalances or copy number variations (CNVs) are a major cause of pregnancy losses, fetal anomalies identified during prenatal period, congenital defects in newborn, dysmorphology and...
    Speaker: Anuradha Udumudi, PhD
    Presented at: APJ Virtual Genetic Solutions Tour 2020
    2
    JUN 19, 2019 | 8:00 AM
    Exploring the genetic landscape of solid tumors using whole-genome copy number analysis
    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
    4
    MAY 09, 2019 | 10:30 AM
    Somatic Gene Recombination in the Brain
    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 and Genomics Virtual Event Series 2019
    2
    MAY 09, 2017 | 8:00 AM
    WEBINAR: Deafness in the Genomic Era: Discoveries, Challenges and Opportunities
    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
    11 8
     
     
  • DEC 06, 2016 | 8:00 AM
    Pre-emptive genotyping for pharmacogenomic risk - establishing a benchmark
    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
    6
    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
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