Partek invites you to join us for educational Webinars on our products to illustrate how they can help accelerate your genomics research.


Learn How to Detect Copy Number Variations in Next Generation Sequencing Data and Integrate with Gene Expression Data

Copy number variations (CNV) are a common form of structural variation, accounting for approximately 10% of human genomic DNA. Although CNVs receive less attention than do single nucleotide variations (SNVs), they are a risk or a protective factor for various diseases and account for differences between individuals. A possible consequence of CNVs is an increase or decrease of expression levels of affected genes, a phenomenon that can be studied by combining DNA-Seq with RNA-Seq data. Join us for a complimentary webinar where we will teach you how to detect copy number variations in your NGS data and how to integrate it into your gene expression study.

Learn how to:
  • Analyzing whole genome sequencing data
  • Detecting amplifications and deletions
  • Interpreting the results through pathway analysis
  • Integrating copy number with gene expression data


July 8, 2015
11:00 a.m. PDT San Francisco
1:00 p.m. CDT Chicago
2:00 p.m. EDT Boston

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July 9, 2015
9:00 a.m. GMT London
10:00 a.m. CEDT Paris
4:00 p.m. SGT Singapore

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Content in both sessions is identical.

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