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.

 

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.