Intended Audience
This webinar is designed for researchers interested in learning how the GDC generates copy number variation (CNV) data and provides an overview of the new GDC Copy Number Segment Tool for visualizing copy number variation over a gene or region. It is ideal for anyone interested in analyzing copy number data for cancer research, regardless of their prior experience in genomics.
Abstract
Join us for an in-depth exploration of the GDC workflows and tools supporting Copy Number Variation (CNV) analysis. This webinar will cover copy number workflows for whole-genome sequencing and SNP array data, including allele-specific segmentation with ASCAT, gene-level CNV profiling with ABSOLUTE, and circular binary segmentation with DNACopy. Data processing steps, output formats, and how the GDC generates CNV data for cancer genomics research will be discussed. This webinar will also demonstrate existing GDC analysis tools for analyzing copy number variation data, as well as the new Copy Number Segment Tool available in the GDC Data Portal for visualizing copy number variation over a gene or regions. A review of GDC CNV Application Programming Interface (API) endpoints for programmatic access will also be provided.
Included Topics
- Overview of GDC workflows for generating copy number segmentation and gene-level copy number data
- Demonstration of GDC tools for visualizing copy number data including the new Copy Number Segment Tool
- Review of the CNV API endpoint for programmatic access
- Live Q&A session to address user questions and gather feedback
Webex Information
Exploring GDC Copy Number Variation (CNV) Analysis Workflows and Tools
- Monday, August 25, 2025
- 2:00 pm | Eastern Standard Time (New York, GMT-04:00) | 1 hr
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