Validation of informCNA using ctDNA in vitro dilutions

The source code for informCNA is available at: https://github.com/nrlab-CRUK/informCNA

The dataset includes a tumor shallow whole-genome sequencing (sWGS) sample and six in vitro diluted plasma cfDNA samples. These cfDNA samples span a gradient of tumor fractions: 10 %, 3.2 %, 1.0 %, 0.32 %, 0.10 %, and 0.032 %.

Each text file contains genomic positions of reads with mappability >30, reported as chromosome and start coordinate.