Genomic Webinar Series

Using Clinical Sequence Analyzer to Solve Rare Diseases

Archived Video

The Use of Clinical Sequence Analyzer (CSA) to Explore Genomic Data on Rare Diseases

01 Aug 2017, 12:00 pm Eastern Time (ET)

Hear the journey of a six year old male with dysmorphic features, developmental delays, and speech regression from initial presentation to final diagnosis. After multiple unrevealing genetic tests, Whole Exome Sequencing (WES) was done and interpreted by Wuxi NextCODE using our Clinical Sequence Analyzer (CSA). The final diagnosis was uncovered in a few minutes and the report generation was done for future family counseling.

Speakers

Katia Meirelles, MDKatia Meirelles, MD Profile Pic

Katia Meirelles, MD
Assistant Director, Medical Geneticist