SFARI Viewer – an online platform to visualize and analyze SFARI genomic data
Tag: Simons Simplex Collection
A genome-wide assessment of noncoding risk variants in autism Olga Troyanskaya, Robert Darnell and colleagues applied deep-learning methods to whole-genome sequencing data from SSC families and identified a clear enrichment for de novo noncoding variation in ASD.
Webinar: SFARI Viewer – an online platform to visualize and analyze SFARI genomic data On June 14, 2019, Alistair Ward and Chase Miller will introduce SFARI Viewer and show how this online platform can be used to visualize and analyze genomic and phenotypic data…
SFARI fall 2018 science meeting highlighted recent findings in autism research SFARI held its fourteenth science meeting September 30–October 2, 2018. SFARI investigators, collaborators and foundation staff came together to discuss recent findings in autism genetics, molecular and system-level mechanisms, as…
SFARI announces Genomic Analysis for Autism Risk Variants in SPARK awardees SFARI announces that it has awarded six grants in response to the Genomic Analysis for Autism Risk Variants in SPARK request for applications. These grants will help to advance the…
Cryptic splice mutations: A major new source of risk variants for neurodevelopmental disorders Kyle Kai-How Farh and Stephan Sanders developed a deep-learning method to predict risk mutations that affect mRNA splicing and contribute substantially to neurodevelopmental disorders.