Validation of informCNA using ctDNA in vitro dilutions
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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.
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Zenodo创建时间：
2026-01-29
