You will find here the python scripts developped for the post-processing analyses reported in the "Sub-diagnostic effects of genetic variants associated with autism" manuscript.
All raw genetic data are available upon request from SFARI-base, UK-Biobank, and downloadable from the Autism Sequencing Consortium and gnomAD. The full variant calling and quality control pipeline is described in details in the manuscript. All phenotypic data for SSC and SPARK cohorts are available upon request from SFARI-base. All functioning/cognitive metrics and MRI-based brain imaging data for UK-Biobank individuals are available upon request from UK-Biobank.