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Explore computational methods for identifying associations between de novo non-coding variants, epigenetic variation, and Autism Spectrum Disorder in this 27-minute conference talk. Learn how to integrate gene expression, sequence, and sex information to uncover connections between non-coding genetic variants and autism. Discover genome-wide approaches for identifying and analyzing recurring patterns of epigenetic variation across individuals. Examine cutting-edge research methodologies that combine multiple data types to better understand the genetic and epigenetic factors contributing to autism spectrum disorders, with insights drawn from recent publications on de novo variant analysis and epigenetic pattern recognition.
