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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, PerkinElmer GenomicsSpeaker information:

Dr. Fen Guo, Ph.D., FACMG, FCCMG

Clinical Laboratory Director, PerkinElmer Genomics

Description

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:

Whole Genome Sequencing

Whole Exome Sequencing

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 genomics@perkinelmer.com.