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Webinars/Presentations

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Webinars and Presentations
Sebastian Dintner
Gerald Martin

September 2, 2020

Enabling Somatic Variant Reporting as a Standard of Care

Guest  Sebastian Dintner, PhD, University of Augsburg
moderator Gerald Martin, PhD, PierianDx

Dr. Sebastian Dintner, Head of Molecular Pathology at the University Hospital of Augsburg, describes how his team is expanding their precision medicine program by enabling genomic testing as a standard of care.
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Amber Leigh, PierianDx
Dale Watkins, PierianDx

August 6, 2020 (Asia Pacific)

Analyzing Complex Genomic Variants

speaker Amber Leigh
moderator Dale Watkins, PhD

In this practice-based webinar, you’ll learn how to analyze complex genomic variants, such as gene fusions, splice-site variants, and co-occurring variants within the context of somatic cancer.  
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Analyzing Complex Genomic Variants in Somatic Cancer
ckwang

July 9, 2020

Using Real-world Data to Improve Cancer Care

guest C.K. Wang, MD, Chief Medical Officer, Cota Healthcare
moderator: Chris Callahan, COO, PierianDx

In this informative webinar, real-world data expert and Chief Medical Officer at Cota Healthcare, Dr. C.K. Wang, describes the value of real-world data and how healthcare institutions can use these data to improve routine cancer care.
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Using Real-world Data to Improve Cancer Care
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erin

June 11, 2020

Validating RUO Assays for Use in Clinical Laboratories

presented by Cates Mallaney and Erin Buck
Moderator: Nabil Hafez

In this educational webinar, we provide best practices for all phases of validating an RUO-based assay to help your clinical laboratory get your NGS test up and running more quickly. 
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Validating Webinar
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May 7, 2020

Streamlining Clinical Genomics Workflows

presented by Mukesh Sharma, PhD, VP Product, and Andy Bredemeyer, PhD, VP Product 

In this webinar, we propose sound strategies for sequencing data transfer, analysis, QC, annotation, interpretation, and reporting that are in wide use by the PierianDx clinical community. Best practices will be demonstrated using Clinical Genomics Workspace and our highly-curated, rules-based Clinical Genomics Knowledgebase for the rapid and accurate identification of actionable clinical variants. 
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Streamlining Clinical Genomics Workflows
Amber Leigh, Field Application Scientist, PierianDx

April 2, 2020

Analyzing Complex Genomic Variants in Somatic Cancer

guest  Amber Leigh, Field Application Scientist
host Gerald Martin, PhD, Field Application Scientist

In this practice-based webinar, you’ll learn how to analyze complex genomic variants, such as gene fusions,  splice-site variants, and co-occurring variants within the context of somatic cancer.  
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Analyzing Complex Genomic Variants in Somatic CAncer
linderpix-BostonHealthcare-9530-web Joseph Ferrara (1)

December 12, 2019

2020 NGS Testing Reimbursement Overview

guest Josepha Ferrara, President, Boston Healthcare
host Michael Sanderson, CEO, PierianDX

In this informative webinar, PierianDx and Boston Healthcare examine the evolving landscape of NGS test reimbursement and provide strategies for improving the level at which your organization is reimbursed.
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2020 NGS Testing Reimbursement Overview
Rakesh Nagarajan

September 25, 2019

Enabling Comprehensive Genomic Profiling in Your Laboratory

guest Rakesh Nagarajan, MD, PhD, Founder, PierianDx
host Michael Schubert, The Pathologist

In this informative webinar we will explore how your laboratory can prepare to offer comprehensive genomic profiling assays by discussing strategies for validation, implementation, and reporting. 
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Enabling Comrpehensive Genomic Profiling The Pathologist
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June 27, 2019

Maximizing the Clinical Utility of Next Generation Sequencing

guest Eric Vail, MD, Director of Molecular Pathology, Cedars-Sinai and Rakesh Nagarajan, MD, PhD, Founder, PierianDx
host OncLive

In this informative webinar, Eric Vail, MD, director of molecular pathology, Cedars-Sinai Medical Center, will discuss how testing programs have positively transformed patient care. Vail will also explain how organizations can maximize the clinical utility of patient reports by leveraging electronic medical record data and standardizing interpretation language.
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Maximizing the Clinical Utility of Next Generation Sequencing
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April 24, 2019

Enabling Comprehensive Genomic Profiling Genomic Profiling with TruSight Oncology 500

guest Rakesh Nagarajan, MD, PhD, Founder, PierianDx
host PierianDx

In this educational webinar, we explore how your laboratory can rapidly validate, implement, and report using the pan cancer profiling assay.   
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Amber Leigh

February 21, 2019

Analyzing Complex Genomic Variants in Somatic Cancer

guest Amber Leigh, Application Scientist
host PierianDx

In this practice-based webinar, you’ll learn how to analyze complex genomic alterations, such as gene fusions, splice-site mutations, and co-occurring variants within the context of somatic cancer.  
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Analyzing Complex Genomic Variants in Somatic Cancer
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January 21, 2019

Building a Clinical NGS Testing Program

guest: Rakesh Nagarajan, MD, PhD
host: Precision Medicine World Conference 2019

PierianDx Founder and Executive Chairman, Rakesh Nagarajan, highlights strategic considerations for building an effective clinical NGS testing menu that achieves greater control, cost savings, and better care for patients.
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Joseph Ferrara, Boston Healthcare

December 18, 2019

Navigating the Reimbursement Landscape for Clinical Next Generation Sequencing

guest Josepha Ferrara, President, Boston Healthcare
host Michael Sanderson, CEO, PierianDx

In this informative webinar, PierianDx and Boston Healthcare dissect the evolving landscape of NGS test reimbursement. We will provide a toolkit that enables molecular diagnostic laboratories to demonstrate the clinical utility of a test, effectively bill for the test, and communicate value to payors--all to improve reimbursement.
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November 29, 2018

Supporting NGS-based IVD Assays with the Most Accurate, Comprehensive, and Clinically Robust Knowledgebase

guests: Rakesh Nagarajan, MD, PhD
host: Association for Molecular Pathology Annual Meeting, 2018

Clinical NGS has been widely adopted as Laboratory Derived Tests (LDTs). NGS-based in vitro diagnostics (IVD) recently gained FDA approval with many others now in process. These IVD assays facilitate broad, widespread adoption of NGS-based testing globally in cancer and other complex conditions that require timely, accurate diagnoses and treatment. To support comprehensive interpretation of these assays, we have developed the PierianDx KnowledgeBase. Driven by the richest set of curated and rationalized content of medical interpretations, clinical practice guidelines, FDA therapeutics and clinical trials, the PierianDx KnowledgeBase offers the most well-vetted interpretations and classifications of genomic variants for IVD use.
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August 28, 2018

CAP Distributive Model of NGS Testing: A Rapid, Economical Approach to Building Your NGS Program

guests: Shalini Verma, MD, FCAP; and Karl Voelkerding, MD, FCAP
host: Rakesh Nagarjan, MD, PhD

Optimism for next generation sequencing (NGS) technologies to be used in a clinical setting quickly turns to numerous conversations about the challenges involved. In this webinar, we discuss the CAP (College of American Pathologists) Distributive Model and how your organization can leverage it to rapidly and economically conduct or scale clinical NGS testing.
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July 19, 2018

A Practice-based Guide to Interpretation and Reporting of Sequence Variants in Cancer

guests: Shalini Verma, MD, FCAP; Andy Bredemeyer, PhD
host: Josh Forsythe

Broader adoption of next-generation sequencing-based cancer testing reveals the challenges associated with variant interpretation and underscores the need to standardize results across molecular pathology labs. Guidelines developed by the Association for Molecular Pathology (AMP) with representation from key institutions, including ACMG, outline a system to categorize sequence variations in cancer.
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May 31, 2018

Bringing NGS Testing In-House

guests: Eric Loo, MD and Rakesh Nagarjan, MD, PhD
host: Josh Forsythe

Dartmouth-Hitchcock has experienced nearly 40% savings by bringing NGS testing in-house. A recent AMP study using non-small cell lung cancer as an example cites $2.7 million in anticipated savings. In-house NGS testing is the foundation of any modern precision medicine program. It can have a profound effect on patient care. And, as these examples show, a strong business case can be made.
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February 22, 2018

Panel Discussion Regarding Debated CMS National Coverage Decision on NGS Testing

guests:  Ravindra Kolhe, MD, PhD; Karen L. Kaul, MD, PhD; Theresa Ann Boyle, MD, PhD; Mani S. Mahadevan, MD; and Nikoletta Sidiropoulos, MD
hosts: Rakesh Nagarjan, MD, PhD, and Shalini Verma, MD,FCAP

How do recent coverage decisions on NGS testing affect you? For academic centers, leading cancer institutions, and essential community cancer centers that have CLIA-certified laboratories providing validated laboratory developed NGS-based tests, the policy would supersede existing local coverage policies for most of those tests and limit Medicare beneficiaries’ access to a single test.
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October 12, 2017

Precision Oncology Roundtable: Ask the Experts about NGS-based Tumor Profiling

guests: Gregory Tsongalis, MD; Anthony Magliocco, MD; and Ravindra Kolhe, MD
hosts: GenomeWeb and PierianDx

The TST170 next-generation sequencing-based panel targets single nucleotide variants, indels, gene amplifications, gene fusions, splice variants, mRNA expression, and mRNA isoform detection found in 170 cancer-related genes and also calculates metrics such as tumor mutation burden and determines evidence for microsatellite instability. Panelists discuss the design of the assay, data analytics, and reasons behind their selection of the TST170 assay, and will share details of how it is being utilized within their organizations.
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January 21th, 2017

Clinical Genomics Workspace (CGW): Accelerate Your NGS Testing with an End-to-End Integrated Workspace

guest: Rakesh Nagarajan
host: PierianDx

PierianDx accelerates precision medicine by offering one space to handle a range of genomic testing, from somatic to constitutional, from small panels to whole exome or genome. During this webinar, PierianDx Chief Biomedical Informatics Officer Dr. Rakesh Nagarajan will provide an overview of CGW and illustrate how the industry leading platform seamlessly manages genomic data and workflow for each case, from variant analysis and classification to interpretation, reporting and final sign out.

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September 14, 2017

Building a Best-in-Class Precision Medicine Program: The Moffitt Cancer Center Story

guest: Anthony Magliocco, MD
host: Rakesh Nagarajan, MD, PhD

Building a world-class precision medicine program takes the right mix of innovative leadership, advanced technology, clinical acumen, and strategic partnerships. During this webinar, Dr. Anthony Magliocco, the Chair of Anatomic Pathology at Moffitt Cancer Center, will share the Moffitt success story – from its pioneering inception to being one of only 47 Comprehensive Cancer Centers as designated by the National Cancer Institute.
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July 13, 2017

Taking Your NGS Testing Program to the Next Level with Enhanced Validation and Interpretation Services

guest: Rakesh Nagarajan
host: PierianDx

The success of any precision medicine program involves the right combination of personnel and technology. PierianDx’s Clinical Genomicist Workspace (CGW) has been the technology platform of choice for clinical labs to seamlessly manage their genomic data and workflow from variant analysis and classification to interpretation, reporting and final sign out. However, the right strategy and clinical resources at the validation and interpretation stages are just as important to that success. During this webinar, PierianDx Chief Bioinformatics Officer Rakesh Nagarajan will discuss ways clinical labs can improve validation and interpretation approaches to enhance report actionability, relevance and throughput.
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March 9, 2017

Accelerating Your NGS Testing Program: Examples and Case Studies

guest: Nikoletta Sidiropoulos, MD
host: PierianDx

Dr. Sidiropoulos shared her experiences and lessons learned as she works to evolve the university’s precision medicine program. Specific examples were shared on how to improve clinical lab workflow, starting with DNA or RNA samples and ending with a report of relevant variants to assist in clinical decision-making. By the end of this webinar, participants will have some real-world examples of how to accelerate their own personalized medicine initiatives from clinical experts in the field.
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December 21, 2017

NGS Roundtable: Ask the Experts about the Future of Clinical NGS Testing

guests: Allie Grossman, MD; Karl Voelkerding, MD, FCAP; and Rakesh Nagarajan, MD, PhD
host: GenomeWeb

This interactive roundtable discusses established and emerging regulatory, scientific, and medical topics related to next-generation sequencing in the clinical setting. An expert panel of leading pathologists, medical geneticists, and researchers will address genomic testing advances in two thematic areas: 1) scientific and clinical trends in reporting, and 2) clinical lab operations and quality management.
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January 12, 2017

Practice Guidelines and Clinical Trials in CGW

guest:  Andy Bredemeyer, PhD
host: PierianDx

Learn more about the knowledgebase and how PierianDx annotates practice guidelines and clinical trials.

 
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