Audience: This webinar is geared towards those involved with genomic variation analysis and interpretation of copy number variation (CNV) from next-generation sequencing (NGS) data in cytogenetics or molecular genetics labs.
Dr. Fen Guo, Ph.D., FACMG, FCCMG
Clinical Laboratory Director, PerkinElmer Genomics
In this one-hour webinar Dr. Guo will:
- Introduce the main methods utilized for the detection of copy number variants (CNV) using next-generation sequencing (NGS) data
- Share clinical cases to illustrate how coverage and uniformity of NGS data contribute to the resolution of CNV calling
Featured PerkinElmer Genomic assays include:
CNGnome® (detects large copy number changes throughout the genome)
For more information on how to order genomic testing from PerkinElmer Genomics please call 866-354-2910 or email email@example.com.