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    ChIP-Sequencing

    ChIP-Sequencing: a method used to analyze protein interactions with DNA. ChIP-seq combines chromatin immunoprecipitation with massively parallel DNA sequencing to identify the binding sites of DNA-associated proteins.

    Webinars

    • 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
      NOV 11, 2015 | 12:00 PM
      DNASTAR Software for Accurate Variant Detection and Validation in Targeted Gene Panel Data Sets
      DNASTAR Software for Accurate Variant Detection and Validation...
      DNASTAR offers an integrated suite of software for accurate assembly, alignment, and analysis of sequence data from all major next-generation sequencing platforms, supporting key workflows in...
      Speaker: Matthew Keyser, MS
      Presented at: Clinical Diagnostics & Research Virtual Event Series 2015
      0
      OCT 28, 2015 | 11:00 AM
      The Hidden Effects of Epigenetic Discoveries
      The Hidden Effects of Epigenetic Discoveries
      DATE: October 28th, 2015TIME: 11am Pacific time, 2pm Eastern timeNew discoveries uncover that exposure to current environmental, dietary, behavioral, and medical conditions can significantly...
      Speaker: Jeffrey Kim, PhD , Christopher Scharer, PhD , Carlos Barrero, MD
      Sponsored By: Rockland
      25
      SEP 30, 2015 | 12:00 PM
      Modeling and dissecting hepatocellular carcinoma dissemination
      Modeling and dissecting hepatocellular carcinoma dissemination
      Hepatocellular carcinoma (HCC) is a significant contributor to cancer-related mortality in the United States and worldwide. Current treatments are largely ineffective: single agent and combin...
      Speaker: Brian Lewis, PhD
      Presented at: Cancer Research & Oncology Week Virtual Event Series 2015
      2
      SEP 02, 2015 | 12:00 PM
      DNASTAR Software for Assembly and Analysis of Microbial Genomes
      DNASTAR Software for Assembly and Analysis of Microbial Genomes
      DNASTAR offers an integrated suite of software for accurate assembly and analysis of sequence data for key NGS workflows, including microbial genome assembly. The DNASTAR assembly software is...
      Speaker: Matthew Keyser, MS
      Presented at: Microbiology Virtual Event Series 2015
      3
      JUN 11, 2015 | 11:00 AM
      Assessing Quality Using ACCURUN® Controls for Quantitative Viral Load Assays
      Assessing Quality Using ACCURUN® Controls for Quantitative Viral...
      Consistent accuracy in reporting quantitative viral load results is critically important to patients, their physicians and to the clinical laboratory. In clinical practice, quantitative viral...
      Speaker: Russell Garlick
      Presented at: Cardinal Health labXchange
      Sponsored By: Cardinal Healthâ„¢ OptiFreight® Logistics
      6
      MAY 14, 2015 | 9:00 AM
      Keynote: Analysis of Complex Diseases Using Integrative Omics
      Keynote: Analysis of Complex Diseases Using Integrative Omics
      I will present new insights into how multiomics profiling can be used to analyze and provide new insights into two complexes diseases, type 2 diabetes and autism....
      Speaker: Michael Snyder, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2015
      4
      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 | 12:00 PM
      DNASTAR Software For Accurate Variant Detection and Validation in Targeted Gene Panel Data Sets
      DNASTAR Software For Accurate Variant Detection and Validation...
      DNASTAR offers an integrated suite of software for accurate assembly and analysis of sequence data from all major next-generation sequencing platforms supporting key workflows including targe...
      Speaker: Matthew Keyser, MS
      Presented at: Genetics and Genomics Virtual Event Series 2015
      2
      SEP 10, 2014 | 10:00 AM
      NGS Lessons in Translational Diagnostics
      NGS Lessons in Translational Diagnostics
      In this webinar, we will describe a comprehensive approach for NGS-based marker discovery and the successful migration of these markers to targeted NGS assays using low-quality (FFPE) and low...
      Speaker: Gary Latham Ph.D. and Brian Haynes, Ph.D.
      Sponsored By: Asuragen, Asuragen
      48
      AUG 21, 2014 | 12:15 PM
      A Next-Gen Sequencing Software Workflow for Gene Panel Validation Control
      A Next-Gen Sequencing Software Workflow for Gene Panel Validation...
      DNASTAR offers an integrated suite of software for assembling and analyzing sequence data from all major next-generation sequencing platforms. DNASTAR software supports a variety of key workf...
      Speaker: Matthew Keyser, MS
      Presented at: Genetics and Genomics Virtual Event Series 2014
      11
      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
      APR 17, 2014 | 11:00 AM
      A Novel Method of Active Paraffin Removal
      A Novel Method of Active Paraffin Removal
        Formalin Fixation and Paraffin Embedding (FFPE) of tissue samples is a routine practice by pathologists; the technique enables high quality preservation of structural information. However, ...
      Speaker: Hamid Khoja, PhD,
      Sponsored By: Covaris, Covaris
      78
      OCT 17, 2013 | 9:00 AM
      Using DNASTAR Software to Identify Cancer Variations in Targeted Resequencing Data
      Using DNASTAR Software to Identify Cancer Variations in Targeted...
      DNASTAR offers an integrated suite of software for assembling and analyzing data from all major next-generation sequencing platforms. The software supports a variety of reference guided and d...
      Speaker: Matthew Keyser, MS
      Presented at: Cancer: Research, Discovery and Therapeutics Virtual Event Series 2013
      48
      AUG 22, 2013 | 10:00 AM
      C.E. CREDITS
      Using Prostate Cancer Exome Data to Identify Candidate Genes
      Using Prostate Cancer Exome Data to Identify Candidate Genes
      In this presentation, exome data from individuals with prostate cancer will be aligned against an annotated reference human genome and SNPs will be identified using DNASTARs SeqMan NGen softw...
      Speaker: Matthew Keyser, MS
      Presented at: Genetics and Genomics Virtual Event Series 2013
      60
      AUG 21, 2013 | 4:00 PM
      C.E. CREDITS
      Development of Targeted Next Generation Sequencing for Pharmacogenomics
      Development of Targeted Next Generation Sequencing for Pharmacogenomics
      The goal of personalized medicine is to customize healthcare to the individual patient. Pharmacogenomics, the analysis of how a patient's genetic makeup affects the individual's response to c...
      Speaker: Edward Ki Yun Leung, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2013
      42
      AUG 21, 2013 | 11:00 AM
      Panel Discussion: Meeting the Demand of Increased NGS Capacity with Automated TruSeq Stranded mRNA Library Preparation
      Panel Discussion: Meeting the Demand of Increased NGS Capacity...
      RNASeq has become the primary method for studying changes in gene expression in modern genomics research. By directly sequencing the various types of RNA molecules, including mRNA, ncRNA, an...
      Speaker: Alisa Jackson, Zach Smith, Mary Blair, Dave Delano
      Presented at: Genetics and Genomics Virtual Event Series 2013
      41
      AUG 21, 2013 | 9:00 AM
      Adventures in Personal Genomics and Whole Omics Profiling
      Adventures in Personal Genomics and Whole Omics Profiling
      Personalized medicine is expected to benefit from the combination of genomic information with the global monitoring of molecular components and physiological states. To ascertain whether this...
      Speaker: Michael Snyder, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2013
      3466
    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
    NOV 11, 2015 | 12:00 PM
    DNASTAR Software for Accurate Variant Detection and Validation in Targeted Gene Panel Data Sets
    DNASTAR Software for Accurate Variant Detection and Validation...
    DNASTAR offers an integrated suite of software for accurate assembly, alignment, and analysis of sequence data from all major next-generation sequencing platforms, supporting key workflows in...
    Speaker: Matthew Keyser, MS
    Presented at: Clinical Diagnostics & Research Virtual Event Series 2015
    0
    OCT 28, 2015 | 11:00 AM
    The Hidden Effects of Epigenetic Discoveries
    The Hidden Effects of Epigenetic Discoveries
    DATE: October 28th, 2015TIME: 11am Pacific time, 2pm Eastern timeNew discoveries uncover that exposure to current environmental, dietary, behavioral, and medical conditions can significantly...
    Speaker: Jeffrey Kim, PhD , Christopher Scharer, PhD , Carlos Barrero, MD
    Sponsored By: Rockland
    25
    SEP 30, 2015 | 12:00 PM
    Modeling and dissecting hepatocellular carcinoma dissemination
    Modeling and dissecting hepatocellular carcinoma dissemination
    Hepatocellular carcinoma (HCC) is a significant contributor to cancer-related mortality in the United States and worldwide. Current treatments are largely ineffective: single agent and combin...
    Speaker: Brian Lewis, PhD
    Presented at: Cancer Research & Oncology Week Virtual Event Series 2015
    2
    SEP 02, 2015 | 12:00 PM
    DNASTAR Software for Assembly and Analysis of Microbial Genomes
    DNASTAR Software for Assembly and Analysis of Microbial Genomes
    DNASTAR offers an integrated suite of software for accurate assembly and analysis of sequence data for key NGS workflows, including microbial genome assembly. The DNASTAR assembly software is...
    Speaker: Matthew Keyser, MS
    Presented at: Microbiology Virtual Event Series 2015
    3
     
     
  • JUN 11, 2015 | 11:00 AM
    Assessing Quality Using ACCURUN® Controls for Quantitative Viral Load Assays
    Assessing Quality Using ACCURUN® Controls for Quantitative Viral...
    Consistent accuracy in reporting quantitative viral load results is critically important to patients, their physicians and to the clinical laboratory. In clinical practice, quantitative viral...
    Speaker: Russell Garlick
    Presented at: Cardinal Health labXchange
    Sponsored By: Cardinal Healthâ„¢ OptiFreight® Logistics
    6
    MAY 14, 2015 | 9:00 AM
    Keynote: Analysis of Complex Diseases Using Integrative Omics
    Keynote: Analysis of Complex Diseases Using Integrative Omics
    I will present new insights into how multiomics profiling can be used to analyze and provide new insights into two complexes diseases, type 2 diabetes and autism....
    Speaker: Michael Snyder, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2015
    4
    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 | 12:00 PM
    DNASTAR Software For Accurate Variant Detection and Validation in Targeted Gene Panel Data Sets
    DNASTAR Software For Accurate Variant Detection and Validation...
    DNASTAR offers an integrated suite of software for accurate assembly and analysis of sequence data from all major next-generation sequencing platforms supporting key workflows including targe...
    Speaker: Matthew Keyser, MS
    Presented at: Genetics and Genomics Virtual Event Series 2015
    2
    SEP 10, 2014 | 10:00 AM
    NGS Lessons in Translational Diagnostics
    NGS Lessons in Translational Diagnostics
    In this webinar, we will describe a comprehensive approach for NGS-based marker discovery and the successful migration of these markers to targeted NGS assays using low-quality (FFPE) and low...
    Speaker: Gary Latham Ph.D. and Brian Haynes, Ph.D.
    Sponsored By: Asuragen, Asuragen
    48
     
     
  • AUG 21, 2014 | 12:15 PM
    A Next-Gen Sequencing Software Workflow for Gene Panel Validation Control
    A Next-Gen Sequencing Software Workflow for Gene Panel Validation...
    DNASTAR offers an integrated suite of software for assembling and analyzing sequence data from all major next-generation sequencing platforms. DNASTAR software supports a variety of key workf...
    Speaker: Matthew Keyser, MS
    Presented at: Genetics and Genomics Virtual Event Series 2014
    11
    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
    APR 17, 2014 | 11:00 AM
    A Novel Method of Active Paraffin Removal
    A Novel Method of Active Paraffin Removal
      Formalin Fixation and Paraffin Embedding (FFPE) of tissue samples is a routine practice by pathologists; the technique enables high quality preservation of structural information. However, ...
    Speaker: Hamid Khoja, PhD,
    Sponsored By: Covaris, Covaris
    78
    OCT 17, 2013 | 9:00 AM
    Using DNASTAR Software to Identify Cancer Variations in Targeted Resequencing Data
    Using DNASTAR Software to Identify Cancer Variations in Targeted...
    DNASTAR offers an integrated suite of software for assembling and analyzing data from all major next-generation sequencing platforms. The software supports a variety of reference guided and d...
    Speaker: Matthew Keyser, MS
    Presented at: Cancer: Research, Discovery and Therapeutics Virtual Event Series 2013
    48
    AUG 22, 2013 | 10:00 AM
    C.E. CREDITS
    Using Prostate Cancer Exome Data to Identify Candidate Genes
    Using Prostate Cancer Exome Data to Identify Candidate Genes
    In this presentation, exome data from individuals with prostate cancer will be aligned against an annotated reference human genome and SNPs will be identified using DNASTARs SeqMan NGen softw...
    Speaker: Matthew Keyser, MS
    Presented at: Genetics and Genomics Virtual Event Series 2013
    60
     
     
  • AUG 21, 2013 | 4:00 PM
    C.E. CREDITS
    Development of Targeted Next Generation Sequencing for Pharmacogenomics
    Development of Targeted Next Generation Sequencing for Pharmacogenomics
    The goal of personalized medicine is to customize healthcare to the individual patient. Pharmacogenomics, the analysis of how a patient's genetic makeup affects the individual's response to c...
    Speaker: Edward Ki Yun Leung, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2013
    42
    AUG 21, 2013 | 11:00 AM
    Panel Discussion: Meeting the Demand of Increased NGS Capacity with Automated TruSeq Stranded mRNA Library Preparation
    Panel Discussion: Meeting the Demand of Increased NGS Capacity...
    RNASeq has become the primary method for studying changes in gene expression in modern genomics research. By directly sequencing the various types of RNA molecules, including mRNA, ncRNA, an...
    Speaker: Alisa Jackson, Zach Smith, Mary Blair, Dave Delano
    Presented at: Genetics and Genomics Virtual Event Series 2013
    41
    AUG 21, 2013 | 9:00 AM
    Adventures in Personal Genomics and Whole Omics Profiling
    Adventures in Personal Genomics and Whole Omics Profiling
    Personalized medicine is expected to benefit from the combination of genomic information with the global monitoring of molecular components and physiological states. To ascertain whether this...
    Speaker: Michael Snyder, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2013
    3466
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