Validation of informCNA using ctDNA in vitro dilutions

Zenodo (CERN European Organization for Nuclear Research) 2026 Dataset Open access

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Authors: Queen Mary University of London
DOI: 10.5281/zenodo.18403943
Cited by: 0

Abstract

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.

Fields of Study & Subjects

Cancer Genomics and Diagnostics Genomic variations and chromosomal abnormalities Genomics and Phylogenetic Studies

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
28 January 2026
Document type
Dataset