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Cancer Genomics ONLINE - Webinar 1: Interrogating and targeting the complexities of the cancer genome

About this event

Join us for our latest 3 part webinar series, Cancer Genomics ONLINE to

  • Explore the multi-layered complexities of tumours and their interactions with their environment using advanced omics technologies.
  • Discover new ways in which cancer genomics is being implemented in the clinic.
  • Learn how epigenetics and methylation signatures are aiding cancer detection.

Webinar 1: Interrogating and targeting the complexities of the cancer genome

Tuesday 5th July, 3pm BST/ 4pm CET/ 10am EST

Since the discovery of the “cancer genome,” we have increasingly become aware of its complexities and its interactions with the microenvironment, the immune system, drivers of metastasis and beyond.

In this webinar, we will highlight how advanced omics technologies are unravelling the complexities of the cancer genome and beyond; and highlight how these are providing insights that could translate to actionable insights.

Using machine learning to predict driver variants in the human cancer genome – Colin Campbell, Reader in Mathematics for Information Technology, University of Bristol

Spatial CRISPR genomics identifies regulators of the tumor microenvironment – Brian Brown, Director, Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, Mount Sinai Medical Center

Targeting oncogenic long noncoding RNAs for cancer therapy – Tao Liu, Associate Professor & Group Leader – Gene Dysregulation Group, Children's Cancer Institute Australia, The University of New South Wales

Webinar 2: Clinical cancer genomics in 2022 and beyond

12th July, 3pm BST/ 4pm CET/ 10am EST

Despite the advances in next-generation sequencing, opportunities remain to better utilise genomic capabilities for cancer detection, characterisation, and monitoring.

This webinar will cover the latest in robust sequencing of cancers in the clinics, and how we can scale up our capabilities to better support patients going forward.

Improving accuracy and consistency of variant interpretation for cancer susceptibility genes – Alice Garrett, Clinical Research Fellow, Institute of Cancer Research

Lab Automation for Cancer Genomics: Work Smarter – Craig Johnston, Diagnostics & Genomics Lead, Automata

Integrating whole genome sequencing into clinical practice for cancer patients – Alona Sosinsky, Scientific Director of Cancer, Genomics England

Webinar 3: Cancer epigenetics and detecting methylation signatures

19th July, 3pm BST/ 4pm CET/ 10am EST

With DNA methylation being long regarded as a hallmark of cancer, recent advances in detection technology have shown great promise in the utility of using methylation status as a tool to diagnose cancer early. However, translating these into the clinic remains slow.

In this webinar, we highlight advances in “going beyond the genome” for cancer diagnostics and address the challenges of widespread clinical utility.

The Promise of Multicancer Early Detection – Eric Klein, Member, Population and Cancer Prevention Program, Case Comprehensive Cancer Center, Case Western Reserve University

Leading the way in target enrichment: Exceptional performance, improved efficiency and rapid customization of targeted methylation sequencing - Bryan N. Höglund, Senior Manager - NGS Business Development, Twist Bioscience

DNA methylation age as a biomarker for cancer - Chungho Lau, Research Associate, Imperial College London

mDETECT, a suite of second generation liquid biopsies for multiple cancers – Christopher Mueller, Professor, Queen's Cancer Research Institute, Queen’s University

Hosted by

  • Guest speaker
    BB G
    Brian Brown

  • Guest speaker
    CC G
    Colin Campbell

  • Guest speaker
    TL G
    Tao Liu

  • Team member
    DG T
    Diana Georgi Front Line Genomics

Front Line Genomics

Delivering the Benefits of Genomics to Patients Faster

Front Line Genomics is a genomics-focused media company, with a social mission to deliver the benefits of genomics to patients faster. We organise the Festival of Genomics, digital events and webinars. We also produce reports and operate a content-rich website.