Presenter: Rebecca Laborde, PhD.
Field Application Scientist, Regional Marketing Clinical and Translational Medicine
Many Patients that suffer from neurological deficiencies face delays in receiving an accurate diagnosis for their symptoms and effective treatment due to the diverse range of possible causes for their phenotype.
There are a variety of neurological disorders that present with very similar symptoms with causes ranging from disease, toxin exposure and injury to acquired or inherited genetic factors. This complicated clinical landscape presents physicians with the challenge of determining which factors are most significantly contributing to the patient’s symptoms. The application of genomic sequencing (NGS) is becoming increasingly popular as an approach to clarify the causes of neurological disorders. These genomic studies produce large datasets that must be integrated with clinical data to inform physicians of the underlying cause of disease.
In this webinar, we will examine datasets that showcase the power of Spotfire® in integrating genomic data with patient clinical data. We will demonstrate the power of combined visualizations for their ability to uncover patterns between genomic and clinical data. Simplifying these integrative data analysis techniques remains at the center of translational medicine and PerkinElmer is uniquely positioned in this space to provide solutions for data generation and integrated analysis.
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