Results for “wgs”

Calculate polygenic risk scores from direct-to-consumer genetic data using published scoring files from the PGS Catalog and contextualize results against population reference distributions.

Takes raw whole-genome sequencing FASTQ files or a pre-existing VCF through variant calling, quality control, and polygenic risk score computation using the PGS Catalog.

Calculates polygenic risk scores from 23andMe or AncestryDNA genotype files using PGS Catalog scoring files, then estimates population percentiles and risk categories.

Read and write Google Sheets spreadsheets using the gws CLI, including batch updates, creation, and data retrieval.

Automates genome-wide association studies from genotype files to publication-ready results, running PLINK2 QC and REGENIE regression with Manhattan and QQ plots.

Generates audit logs and usage reports for Google Workspace accounts via the Admin SDK Reports API.

Queries 9 genomic databases in parallel for a given rsID, returning unified GWAS, PheWAS, eQTL, and fine-mapping reports.

Reads cell values from a Google Sheets spreadsheet by ID and range using the gws CLI.