Tha dataset includes whole-genome sequencing of a cohort of patients with non-small lung cancer. All these patients have no or very limited smoking history.
BackgroundCopy number variations (CNVs) represent an important type of genetic variation that deeply impact phenotypic polymorphisms and human diseases. The advent of high-throughput sequencing techno
A gzipped tarball containing a directory holding multiple FASTQ files. Each file contains reads from a single genotyped individual, with genotyping carried out using low pass Whole Genome Sequencing (
