Genome of Switzerland Pilot: Genomic Sequences

This FASTQ dataset contains raw sequencing reads from participants included in the Genome of Switzerland Pilot. It represents the primary sequence-level output generated before alignment and variant calling, and supports downstream genome analysis including quality control, read alignment, variant discovery, allele-frequency estimation, population-structure analysis, and pharmacogenomic research. The dataset is intended to enable research on genomic variation within the contemporary Swiss population starting from the raw sequencing data.