Webinar Recording Available All Levels Dr. Omics

Precision at Scale: Unlocking the Potential of Targeted NGS Webinar by Thermofisher Scientific

Accelerate clinical breakthroughs with high-throughput targeted NGS workflows. Learn scalable precision medicine strategies from industry pioneers at Thermo Fisher Scientific and Dr. Omics Edu.

  • 5.0/5
  • English
  • Updated Aug 2026
Precision at Scale: Unlocking the Potential of Targeted NGS Webinar by Thermofisher Scientific

About this course

This exclusive, free webinar explores the frontier of genomic medicine through the lens of Targeted Next-Generation Sequencing (NGS). As precision oncology and personalized healthcare demand higher accuracy and throughput, understanding scalable genomic workflows becomes critical. Hosted by Dr. Omics Edu in collaboration with Thermo Fisher Scientific, this session breaks down the technical complexities of deep sequencing, variant calling, and panel design. Participants will explore how targeted panels maximize sequencing depth while minimizing operational costs and data-analysis bottlenecks. Our expert speakers will dissect real-world case studies demonstrating precision at scale, from sample preparation to clinical bioinformatics interpretation. Whether you are aiming to optimize your laboratory’s assay pipelines or understand the latest market trends in molecular diagnostics, this masterclass provides the foundational and advanced insights necessary to drive impactful life science research.

What you will learn

The core principles of Targeted Next-Generation Sequencing versus whole-genome approaches.
Strategies to scale up genomic assays without compromising data precision or analytical sensitivity.
How to leverage Thermo Fisher Scientific solutions for streamlined library preparation and target enrichment.
Bioinformatics pipelines tailored for identifying low-frequency somatic mutations in clinical oncology samples.
Best practices for transitioning from standard molecular assays to high-throughput, automated NGS workflows.

Skills you will gain

NGS-Workflow-Optimization Target-Enrichment Variant-Calling Precision-Oncology Genomic-Bioinformatics Panel-Design Data-Scalability Molecular-Diagnostics
Certification

Available

Issued by Dr. Omics

Course curriculum

1 module

  • Introduction to Precision Medicine and the Evolution of Targeted Sequencing.
  • Deep Dive into Target Enrichment: Hybrid Selection vs. Amplicon-Based Methods.
  • Streamlining the Workflow: From Sample Isolation to High-Throughput Sequencing.
  • Clinical Bioinformatics: Variant Filtering, Annotation, and Interpretation Pipelines.
  • Case Studies in Precision Oncology: Scaling Diagnostics for Impactful Patient Outcomes.
  • Live Q&A and Interactive Panel Discussion with Industry Experts.

What you need to start

  • A foundational understanding of molecular biology, genetics, or DNA structure.
  • Familiarity with basic genomics concepts (experience with standard PCR or sequencing is helpful but not mandatory).

Who this course is for

  • Bioinformaticians & Data Scientists looking to optimize targeted variant-calling pipelines.
  • Oncologists & Clinical Researchers interested in the translational utility of molecular diagnostics.
  • Laboratory Managers & Technicians aiming to scale up their genomic sequencing throughput.
  • Biotech & Life Science Students eager to align their skills with current industry standards.
INR

₹199

₹999 80% off
USD

$5

$20 75% off

Indian learners pay in INR; international learners are billed in USD.

Enroll for International Students

Paying from outside India? Use this link to complete your payment.

This course includes
  • Format Recording Available
  • Level All Levels
  • Language English
  • Modules 1
  • Access 3 months
  • Certificate Yes
  • Provider Dr. Omics
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