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    NGS Oncology

    Next generation sequencing (NGS) is a scientific tool that identifies genetic sequence. When used in oncology, NGS can allow doctors to test the genes in a patient's cancer at the same time, helping to identify an optimal therapeutic option.

    Webinars

    • MAR 23, 2023 | 8:00 AM
      Variant interpretation, literature curation, and clinical trials, oh my! How to simplify somatic NGS analysis & reduce literature review time by 90% with HSMD
      Variant interpretation, literature curation, and clinical trials,...
      Date: March 23, 2023 Time: 8:00am (PDT), 11:00am (EDT), 8:00pm (CEST) Across clinical oncology applications, from molecular testing to cancer research the ability to identify potentially act...
      Speaker: Chelsea Alexander, MS, CGC , Aarthi Goverdhan, PhD
      Sponsored By: QIAGEN
      10
      OCT 19, 2022 | 12:00 PM
      Enabling Sequencing Applications with Improved Transposase-Based Solutions
      Enabling Sequencing Applications with Improved Transposase-Based...
      Date: October 19, 2022 Time: 12:00pm (PDT), 3:00pm (EDT), 9:00pm (CEST) The capacity and speed of modern DNA sequencing platforms has allowed sequencing to become an integral component of bi...
      Speaker: Joseph C. Mellor, Ph.D. , Curtis Knox , Jessica Smith, Ph.D.
      Sponsored By: seqWell
      10
      SEP 06, 2022 | 10:00 AM
      Techniques and Tips: Learn Sample Preparation for Next Generation Sequencing
      Techniques and Tips: Learn Sample Preparation for Next Generation...
      Date: September 06, 2022 Time: 10:00am (PDT), 1:00pm (EDT), 7:00pm (CEST) Next Generation Sequencing (NGS) provides comprehensive genomic information about disease, development, and other bi...
      Speaker: Thilanka Jayaweera , Juili Kelvekar , Andrew Dix
      Sponsored By: Thermo Fisher Scientific
      29
      AUG 24, 2022 | 8:00 AM
      Oncomine Reporter - Integrated Reporting for Solid Tumor and Myeloid Somatic Variants
      Oncomine Reporter - Integrated Reporting for Solid Tumor and Myeloid...
      Date: August 24, 2022 Time: 8:00am (PDT), 11:00am (EDT), 5:00pm (CEST) Next Generation Sequencing (NGS) has evolved rapidly since the first sequencing platforms were commercially released ne...
      Speaker: Dr. David Seidman, Ph.D., MB (ASCP)
      Sponsored By: Thermo Fisher Scientific
      16
      MAY 11, 2022 | 12:00 PM
      Conserving California: Applying Whole Genome Sequencing in the California Conservation Genomics Project (CCGP)
      Conserving California: Applying Whole Genome Sequencing in the...
      Date: May 11, 2022 Time: 12:00pm (PDT), 3:00pm (EDT), 9:00pm (CEST) In this presentation, Dr. Courtney Miller and Daniel Rodrigues Oliveira, M.S. will describe the efforts of the California...
      Speaker: Daniel Rodrigues Oliveira, M.S. , Courtney Miller, Ph.D. , Ariele Hanek, Ph.D.
      Sponsored By: seqWell
      15
      APR 19, 2022 | 5:30 AM
      Delivering Fast, Flexible Next-Generation Sequencing through Innovations in Chemistry and Engineering
      Delivering Fast, Flexible Next-Generation Sequencing through Innovations...
      Next-generation sequencing (NGS) has become a foundational tool for both biological research and in-vitro diagnostics, particularly in oncology, immunology, and detection of genetic disorder...
      Speaker: Timothy Looney, PhD
      Presented at: Genetics Week Virtual Event Series 2022
      3
      MAR 30, 2022 | 6:00 AM
      Announcing the launch of the Genexus Dx Integrated Sequencer (CE-IVD) - nucleic acid to NGS report in as little as 24 hours
      Announcing the launch of the Genexus Dx Integrated Sequencer (CE-IVD)...
      Targeted NGS has been instrumental in helping the healthcare community deliver on the promise of precision medicine. The Ion Torrent Genexus Integrated Sequencer has enabled targeted genomic...
      Speaker: Andy Felton, Ph.D. , Dr. Luca Quagliata, PhD, BCMAS , Kathy Davy
      Sponsored By: Thermo Fisher Scientific
      14
      NOV 10, 2021 | 4:30 PM
      Putting the Pieces Together, from Variant Calling to Biological Insights - A Lynch Syndrome Case Study
      Putting the Pieces Together, from Variant Calling to Biological...
      In this webinar, we present a case study on Lynch syndrome (LS), a hereditary condition characterized by a high risk of colorectal cancer, endometrial cancer, and other neoplasia that typica...
      Speaker: Eric Seiser, PhD
      Presented at: Clinical Diagnostics & Research Virtual Event Series 2021
      Sponsored By: QIAGEN
      1
      OCT 07, 2021 | 12:00 PM
      Panel Presentation: Oncology Variant Interpretation Just Got More Precise
      Panel Presentation: Oncology Variant Interpretation Just Got More...
      Across oncology applications, from research to molecular testing and pharmaceutical development, the ability to identify potentially actionable genetic alterations and exploit the molecular...
      Speaker: Beate Litzenburger, Ph.D. , Sheryl Elkin, PhD
      Presented at: Cancer Research & Oncology Week Virtual Event Series 2021
      Sponsored By: QIAGEN
      2
      OCT 06, 2021 | 1:30 PM
      Putting the Pieces Together, from Variant Calling to Biological Insights - A Lynch Syndrome Case Study
      Putting the Pieces Together, from Variant Calling to Biological...
      In this webinar, we present a case study on Lynch syndrome (LS), a hereditary condition characterized by a high risk of colorectal cancer, endometrial cancer, and other neoplasia that typica...
      Speaker: Eric Seiser, PhD
      Presented at: Cancer Research & Oncology Week Virtual Event Series 2021
      Sponsored By: QIAGEN
      2
      APR 29, 2021 | 1:15 PM
      Oncomine Reporter: A Powerful Tool for Oncology NGS Reports
      Oncomine Reporter: A Powerful Tool for Oncology NGS Reports
      Cancer is among the leading causes of death worldwide. In 2018, there were 18.1 million new cases and 9.5 million cancer-related deaths worldwide. With the advancement of next generation seq...
      Speaker: Xia Li, Ph.D., DABMGG, CG(ASCP), FACMG
      Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
      4
      APR 29, 2021 | 12:05 PM
      Point of care NGS in community practice
      Point of care NGS in community practice
      New genomic technologies are changing the face of cancer care, as well as accelerating our biological understanding of cancer. Cris will summarise several parallel cancer initiatives in New...
      Speaker: Brandon Sheffield, MD, FRCPC
      Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
      1
      APR 29, 2021 | 4:35 PM
      Haematological malignancy samples molecular characterization - in a NGS way
      Haematological malignancy samples molecular characterization -...
      Next Generation Sequencing (NGS) based molecular tests have been the one of the major focus for the expansion of molecular service provided by Haemato-oncology Diagnostic Service (HODS) in R...
      Speaker: Lihui Wang, Ph.D.
      Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
      1
      APR 29, 2021 | 4:15 PM
      Comprehensive Genomic Profiling for Homologous Recombination Repair Deficiency (HRD) Assessment
      Comprehensive Genomic Profiling for Homologous Recombination Repair...
      Comprehensive genomic profiling (CGP) is advancing precision oncology research through simultaneous analysis of multiple biomarkers in a single next-generation sequencing (NGS) assay. In thi...
      Speaker: Dr. Andreas Jung
      Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
      2
      APR 29, 2021 | 3:25 PM
      NSCLC molecular profiling: An NGS based approach using Oncomine Solutions
      NSCLC molecular profiling: An NGS based approach using Oncomine...
      Next-generation sequencing is transforming scientific research and testing. Thanks to large-scale cancer projects (e.g. The Cancer Genome Atlas - TCGA), the accumulated knowledge is now used...
      Speaker: Artur Kowalik, Ph.D.
      Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
      3
      APR 22, 2021 | 10:30 AM
      Extraction-free sensitive detection of viral RNA using direct RT-PCR chemistry
      Extraction-free sensitive detection of viral RNA using direct...
      Nucleic acid amplification tests (NAAT) are a reliable, sensitive, and accurate diagnostic approach used in viral detection. The approach involves the isolation of nucleic acids from a sampl...
      Speaker: Donald Green
      Presented at: Genetics Week Virtual Event Series 2021
      Sponsored By: Cytiva
      4 1
      APR 22, 2021 | 6:00 AM
      Panel Presentation: Powering the precision in "precision medicine" - The role of curated data, databases and knowledge: Does a gold standard exist?
      Panel Presentation: Powering the precision in "precision medicine"...
      As NGS panels grow, test interpretation becomes more complex and time-consuming / With the explosion of NGS data, the need for consolidated databases with reliable and transparent curation a...
      Speaker: Dominic John , Simon Forbes, PhD , Shawn Bauer , Lisa Barrow-Laing
      Presented at: Genetics Week Virtual Event Series 2021
      Sponsored By: QIAGEN
      2
      APR 22, 2021 | 12:00 AM
      An Introduction to Resources Facilitating Cancer Variant Interpretation
      An Introduction to Resources Facilitating Cancer Variant Interpretation
      Learning Objectives: 1. Identify different kinds of genomic resources 2. Learn to apply the features available in genomic resources to cancer variant interpretation 3. Describe the importanc...
      Speaker: Beth Pitel, M.S., CG(ASCP)CM
      Presented at: Genetics Week Virtual Event Series 2021
      2
      APR 21, 2021 | 7:30 AM
      Panel Presentation: Next-Generation Sequencing in the Global Response to the COVID-19 Pandemic
      Panel Presentation: Next-Generation Sequencing in the Global Response...
      The SARS-CoV-2 pandemic is challenging our health care systems and has profoundly impacted our society. Due to the poor global public health response, SARS-CoV-2 has developed many variants....
      Speaker: Eric Allen, MBA, M. Eng. Bioengineering , Michael Oberholzer, PhD
      Presented at: Genetics Week Virtual Event Series 2021
      2
      APR 21, 2021 | 12:00 AM
      Liquid Biopsy-based Detection of Early Stage Gynecological Cancers
      Liquid Biopsy-based Detection of Early Stage Gynecological Cancers
      According to the American Cancer Society, in there were an estimated 110,070 new cases diagnosed and approximately 32,120 deaths from gynecologic cancers in the U.S. in 2018. Of the five mos...
      Speaker: Lesley E. Northrop, PhD, FACMG
      Presented at: Genetics Week Virtual Event Series 2021
      2
      APR 21, 2021 | 12:00 AM
      Flex Analysis: A Safe, Integrated and Flexible Approach to Non-Invasive Aneuploidy Analysis
      Flex Analysis: A Safe, Integrated and Flexible Approach to Non-Invasive...
      NGS Bioinformatics software has come of age. Our workflows need software solutions that don’t only carry out the correct calculations to give the correct results reliably and unambiguo...
      Speaker: Matthew C. Forman, PhD
      Presented at: Genetics Week Virtual Event Series 2021
      1
      APR 20, 2021 | 3:00 PM
      Panel Presentation: Accelerating precision oncology with matched FFPE and plasma biospecimens characterized using Discovery's SpecimenSeqâ„¢ NGS Service and QIAGEN's QIAseq Multimodal Panels
      Panel Presentation: Accelerating precision oncology with matched...
      Bridging a deep understanding of molecular profiles with clinical information is critical to developing innovative precision medicine tools in oncology. Discovery’s recently launched S...
      Speaker: Nathan Henson, MS , Donald Skifter, PhD, MBA
      Presented at: Genetics Week Virtual Event Series 2021
      Sponsored By: QIAGEN
      2
      APR 14, 2021 | 1:30 PM
      Automated Solutions for SARS-CoV-2 Variant Identification and Surveillance
      Automated Solutions for SARS-CoV-2 Variant Identification and...
      Several SARS-CoV-2 variants are circulating globally. The most prominent variants of concern, including the B.1.1.7, B.1.351 and B1.1.28 lineages, not only carry a constellation of genetic m...
      Speaker: Anthony Tong, PhD , Subodh Nimkar
      Presented at: Coronavirus Series
      Sponsored By: BGI Americas
      3
      NOV 12, 2020 | 3:00 PM
      Translating insights into better outcomes: The new QIAseq Human Exome integrated solution
      Translating insights into better outcomes: The new QIAseq Human...
      What if your lab could perform exome sequencing with the same sensitivity and efficiency of targeted sequencing? The new integrated QIAseq Human Exome TR Insights solution from QIAGEN delive...
      Speaker: Brian Dugan, M.S. , Rupert Yip, PhD
      Presented at: Clinical Diagnostics & Research Virtual Event Series 2020
      Sponsored By: QIAGEN
      1
    MAR 23, 2023 | 8:00 AM
    Variant interpretation, literature curation, and clinical trials, oh my! How to simplify somatic NGS analysis & reduce literature review time by 90% with HSMD
    Variant interpretation, literature curation, and clinical trials,...
    Date: March 23, 2023 Time: 8:00am (PDT), 11:00am (EDT), 8:00pm (CEST) Across clinical oncology applications, from molecular testing to cancer research the ability to identify potentially act...
    Speaker: Chelsea Alexander, MS, CGC , Aarthi Goverdhan, PhD
    Sponsored By: QIAGEN
    10
    OCT 19, 2022 | 12:00 PM
    Enabling Sequencing Applications with Improved Transposase-Based Solutions
    Enabling Sequencing Applications with Improved Transposase-Based...
    Date: October 19, 2022 Time: 12:00pm (PDT), 3:00pm (EDT), 9:00pm (CEST) The capacity and speed of modern DNA sequencing platforms has allowed sequencing to become an integral component of bi...
    Speaker: Joseph C. Mellor, Ph.D. , Curtis Knox , Jessica Smith, Ph.D.
    Sponsored By: seqWell
    10
    SEP 06, 2022 | 10:00 AM
    Techniques and Tips: Learn Sample Preparation for Next Generation Sequencing
    Techniques and Tips: Learn Sample Preparation for Next Generation...
    Date: September 06, 2022 Time: 10:00am (PDT), 1:00pm (EDT), 7:00pm (CEST) Next Generation Sequencing (NGS) provides comprehensive genomic information about disease, development, and other bi...
    Speaker: Thilanka Jayaweera , Juili Kelvekar , Andrew Dix
    Sponsored By: Thermo Fisher Scientific
    29
    AUG 24, 2022 | 8:00 AM
    Oncomine Reporter - Integrated Reporting for Solid Tumor and Myeloid Somatic Variants
    Oncomine Reporter - Integrated Reporting for Solid Tumor and Myeloid...
    Date: August 24, 2022 Time: 8:00am (PDT), 11:00am (EDT), 5:00pm (CEST) Next Generation Sequencing (NGS) has evolved rapidly since the first sequencing platforms were commercially released ne...
    Speaker: Dr. David Seidman, Ph.D., MB (ASCP)
    Sponsored By: Thermo Fisher Scientific
    16
    MAY 11, 2022 | 12:00 PM
    Conserving California: Applying Whole Genome Sequencing in the California Conservation Genomics Project (CCGP)
    Conserving California: Applying Whole Genome Sequencing in the...
    Date: May 11, 2022 Time: 12:00pm (PDT), 3:00pm (EDT), 9:00pm (CEST) In this presentation, Dr. Courtney Miller and Daniel Rodrigues Oliveira, M.S. will describe the efforts of the California...
    Speaker: Daniel Rodrigues Oliveira, M.S. , Courtney Miller, Ph.D. , Ariele Hanek, Ph.D.
    Sponsored By: seqWell
    15
     
     
  • APR 19, 2022 | 5:30 AM
    Delivering Fast, Flexible Next-Generation Sequencing through Innovations in Chemistry and Engineering
    Delivering Fast, Flexible Next-Generation Sequencing through Innovations...
    Next-generation sequencing (NGS) has become a foundational tool for both biological research and in-vitro diagnostics, particularly in oncology, immunology, and detection of genetic disorder...
    Speaker: Timothy Looney, PhD
    Presented at: Genetics Week Virtual Event Series 2022
    3
    MAR 30, 2022 | 6:00 AM
    Announcing the launch of the Genexus Dx Integrated Sequencer (CE-IVD) - nucleic acid to NGS report in as little as 24 hours
    Announcing the launch of the Genexus Dx Integrated Sequencer (CE-IVD)...
    Targeted NGS has been instrumental in helping the healthcare community deliver on the promise of precision medicine. The Ion Torrent Genexus Integrated Sequencer has enabled targeted genomic...
    Speaker: Andy Felton, Ph.D. , Dr. Luca Quagliata, PhD, BCMAS , Kathy Davy
    Sponsored By: Thermo Fisher Scientific
    14
    NOV 10, 2021 | 4:30 PM
    Putting the Pieces Together, from Variant Calling to Biological Insights - A Lynch Syndrome Case Study
    Putting the Pieces Together, from Variant Calling to Biological...
    In this webinar, we present a case study on Lynch syndrome (LS), a hereditary condition characterized by a high risk of colorectal cancer, endometrial cancer, and other neoplasia that typica...
    Speaker: Eric Seiser, PhD
    Presented at: Clinical Diagnostics & Research Virtual Event Series 2021
    Sponsored By: QIAGEN
    1
    OCT 07, 2021 | 12:00 PM
    Panel Presentation: Oncology Variant Interpretation Just Got More Precise
    Panel Presentation: Oncology Variant Interpretation Just Got More...
    Across oncology applications, from research to molecular testing and pharmaceutical development, the ability to identify potentially actionable genetic alterations and exploit the molecular...
    Speaker: Beate Litzenburger, Ph.D. , Sheryl Elkin, PhD
    Presented at: Cancer Research & Oncology Week Virtual Event Series 2021
    Sponsored By: QIAGEN
    2
    OCT 06, 2021 | 1:30 PM
    Putting the Pieces Together, from Variant Calling to Biological Insights - A Lynch Syndrome Case Study
    Putting the Pieces Together, from Variant Calling to Biological...
    In this webinar, we present a case study on Lynch syndrome (LS), a hereditary condition characterized by a high risk of colorectal cancer, endometrial cancer, and other neoplasia that typica...
    Speaker: Eric Seiser, PhD
    Presented at: Cancer Research & Oncology Week Virtual Event Series 2021
    Sponsored By: QIAGEN
    2
     
     
  • APR 29, 2021 | 1:15 PM
    Oncomine Reporter: A Powerful Tool for Oncology NGS Reports
    Oncomine Reporter: A Powerful Tool for Oncology NGS Reports
    Cancer is among the leading causes of death worldwide. In 2018, there were 18.1 million new cases and 9.5 million cancer-related deaths worldwide. With the advancement of next generation seq...
    Speaker: Xia Li, Ph.D., DABMGG, CG(ASCP), FACMG
    Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
    4
    APR 29, 2021 | 12:05 PM
    Point of care NGS in community practice
    Point of care NGS in community practice
    New genomic technologies are changing the face of cancer care, as well as accelerating our biological understanding of cancer. Cris will summarise several parallel cancer initiatives in New...
    Speaker: Brandon Sheffield, MD, FRCPC
    Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
    1
    APR 29, 2021 | 4:35 PM
    Haematological malignancy samples molecular characterization - in a NGS way
    Haematological malignancy samples molecular characterization -...
    Next Generation Sequencing (NGS) based molecular tests have been the one of the major focus for the expansion of molecular service provided by Haemato-oncology Diagnostic Service (HODS) in R...
    Speaker: Lihui Wang, Ph.D.
    Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
    1
    APR 29, 2021 | 4:15 PM
    Comprehensive Genomic Profiling for Homologous Recombination Repair Deficiency (HRD) Assessment
    Comprehensive Genomic Profiling for Homologous Recombination Repair...
    Comprehensive genomic profiling (CGP) is advancing precision oncology research through simultaneous analysis of multiple biomarkers in a single next-generation sequencing (NGS) assay. In thi...
    Speaker: Dr. Andreas Jung
    Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
    2
    APR 29, 2021 | 3:25 PM
    NSCLC molecular profiling: An NGS based approach using Oncomine Solutions
    NSCLC molecular profiling: An NGS based approach using Oncomine...
    Next-generation sequencing is transforming scientific research and testing. Thanks to large-scale cancer projects (e.g. The Cancer Genome Atlas - TCGA), the accumulated knowledge is now used...
    Speaker: Artur Kowalik, Ph.D.
    Presented at: OncomineWorld 2022: A Virtual NGS Education Meeting
    3
     
     
  • APR 22, 2021 | 10:30 AM
    Extraction-free sensitive detection of viral RNA using direct RT-PCR chemistry
    Extraction-free sensitive detection of viral RNA using direct...
    Nucleic acid amplification tests (NAAT) are a reliable, sensitive, and accurate diagnostic approach used in viral detection. The approach involves the isolation of nucleic acids from a sampl...
    Speaker: Donald Green
    Presented at: Genetics Week Virtual Event Series 2021
    Sponsored By: Cytiva
    4 1
    APR 22, 2021 | 6:00 AM
    Panel Presentation: Powering the precision in "precision medicine" - The role of curated data, databases and knowledge: Does a gold standard exist?
    Panel Presentation: Powering the precision in "precision medicine"...
    As NGS panels grow, test interpretation becomes more complex and time-consuming / With the explosion of NGS data, the need for consolidated databases with reliable and transparent curation a...
    Speaker: Dominic John , Simon Forbes, PhD , Shawn Bauer , Lisa Barrow-Laing
    Presented at: Genetics Week Virtual Event Series 2021
    Sponsored By: QIAGEN
    2
    APR 22, 2021 | 12:00 AM
    An Introduction to Resources Facilitating Cancer Variant Interpretation
    An Introduction to Resources Facilitating Cancer Variant Interpretation
    Learning Objectives: 1. Identify different kinds of genomic resources 2. Learn to apply the features available in genomic resources to cancer variant interpretation 3. Describe the importanc...
    Speaker: Beth Pitel, M.S., CG(ASCP)CM
    Presented at: Genetics Week Virtual Event Series 2021
    2
    APR 21, 2021 | 7:30 AM
    Panel Presentation: Next-Generation Sequencing in the Global Response to the COVID-19 Pandemic
    Panel Presentation: Next-Generation Sequencing in the Global Response...
    The SARS-CoV-2 pandemic is challenging our health care systems and has profoundly impacted our society. Due to the poor global public health response, SARS-CoV-2 has developed many variants....
    Speaker: Eric Allen, MBA, M. Eng. Bioengineering , Michael Oberholzer, PhD
    Presented at: Genetics Week Virtual Event Series 2021
    2
    APR 21, 2021 | 12:00 AM
    Liquid Biopsy-based Detection of Early Stage Gynecological Cancers
    Liquid Biopsy-based Detection of Early Stage Gynecological Cancers
    According to the American Cancer Society, in there were an estimated 110,070 new cases diagnosed and approximately 32,120 deaths from gynecologic cancers in the U.S. in 2018. Of the five mos...
    Speaker: Lesley E. Northrop, PhD, FACMG
    Presented at: Genetics Week Virtual Event Series 2021
    2
     
     
  • APR 21, 2021 | 12:00 AM
    Flex Analysis: A Safe, Integrated and Flexible Approach to Non-Invasive Aneuploidy Analysis
    Flex Analysis: A Safe, Integrated and Flexible Approach to Non-Invasive...
    NGS Bioinformatics software has come of age. Our workflows need software solutions that don’t only carry out the correct calculations to give the correct results reliably and unambiguo...
    Speaker: Matthew C. Forman, PhD
    Presented at: Genetics Week Virtual Event Series 2021
    1
    APR 20, 2021 | 3:00 PM
    Panel Presentation: Accelerating precision oncology with matched FFPE and plasma biospecimens characterized using Discovery's SpecimenSeqâ„¢ NGS Service and QIAGEN's QIAseq Multimodal Panels
    Panel Presentation: Accelerating precision oncology with matched...
    Bridging a deep understanding of molecular profiles with clinical information is critical to developing innovative precision medicine tools in oncology. Discovery’s recently launched S...
    Speaker: Nathan Henson, MS , Donald Skifter, PhD, MBA
    Presented at: Genetics Week Virtual Event Series 2021
    Sponsored By: QIAGEN
    2
    APR 14, 2021 | 1:30 PM
    Automated Solutions for SARS-CoV-2 Variant Identification and Surveillance
    Automated Solutions for SARS-CoV-2 Variant Identification and...
    Several SARS-CoV-2 variants are circulating globally. The most prominent variants of concern, including the B.1.1.7, B.1.351 and B1.1.28 lineages, not only carry a constellation of genetic m...
    Speaker: Anthony Tong, PhD , Subodh Nimkar
    Presented at: Coronavirus Series
    Sponsored By: BGI Americas
    3
    NOV 12, 2020 | 3:00 PM
    Translating insights into better outcomes: The new QIAseq Human Exome integrated solution
    Translating insights into better outcomes: The new QIAseq Human...
    What if your lab could perform exome sequencing with the same sensitivity and efficiency of targeted sequencing? The new integrated QIAseq Human Exome TR Insights solution from QIAGEN delive...
    Speaker: Brian Dugan, M.S. , Rupert Yip, PhD
    Presented at: Clinical Diagnostics & Research Virtual Event Series 2020
    Sponsored By: QIAGEN
    1
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