Whole-genome and whole-exome sequencing in neurological diseases

Keyphrases

• Whole Genome 100%
• Whole Exome Sequencing 100%
• Neurological Diseases 100%
• Genomic Data 66%
• Genetic Risk 33%
• Counseling 33%
• Common Variants 33%
• Neurological Disorders 33%
• Sequence Variants 33%
• Rare Variants 33%
• Complex Traits 33%
• Clinical Setting 33%
• Structural Variants 33%
• Massively Parallel Sequencing 33%
• Personalized Medicine 33%
• Data Interpretation 33%
• Sift 33%
• Sequencing Technology 33%
• Parsing 33%
• Ethics 33%
• Main Drivers 33%

Biochemistry, Genetics and Molecular Biology

• Exome Sequencing 100%
• Genomics 66%
• Genetic Risk 33%
• Deep Sequencing 33%