CNSistent 1.1.0

CNSistent is a Python tool for processing and analyzing copy number data. It is designed to work with data from a variety of sources. The tool is designed to be easy to use, and to provide a comprehensive set of analyses and visualizations.

READ THE DOCS HERE

CNSistent can be used as a Python package, or downloaded together with the respective data (PCAWG, TRACERx, TCGA, genomic locations):

Installation

Option 1: Full package with the data

git clone git@github.com:ICCB-Cologne/CNSistent.git
cd CNSistent
pip install -e .
wget -O out.tar.gz https://zenodo.org/records/14547456/files/out.tar.gz 
mkdir -p out
tar -xzf out.tar.gz -C ./out 
rm out.tar.gz

Note: the input data are part of the repository. The processed data can be downloaded and decompressed directly as shown above. Alternative is to generate the by running the ./scripts/data_process.sh and ./scripts/data_aggregate.sh.

Option 2: PIP package only

pip install CNSistent

Data

The input dataset is also availble on Zenodo:

The processed data is available on Zenodo:

Deep learning code is available on Zenodo:

Acessions

The contents of the data folder were obtained by processing the following sources, accessed in December 2023.

TCGA data obtained from ASCATv3 at: https://github.com/VanLoo-lab/ascat/tree/master/ReleasedData
Cite: https://www.pnas.org/doi/full/10.1073/pnas.1009843107
The results published here are in part based upon data generated by the TCGA Research Network: https://www.cancer.gov/tcga.

PCAWG data obtained from: https://dcc.icgc.org/releases/PCAWG/consensus_cnv Cite: https://www.nature.com/articles/s41587-019-0055-9

TRACERx data obtained from: https://zenodo.org/records/7649257
Cite: https://www.nature.com/articles/s41586-023-05729-x

COSMIC cancer set obtained from: https://cancer.sanger.ac.uk/census
Cite: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450507

Human genome gene set obtained using PyENSEMBL (2023). Cite: https://academic.oup.com/nar/article/51/D1/D933/6786199

Cytoband, Gap data obtained from: https://genome.ucsc.edu Cite: https://www.nature.com/articles/35057062

Common fragile sites obtained from the HumCFS database: https://webs.iiitd.edu.in/raghava/humcfs/ Cite: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394038 The HumCFS GRCh38/hg38 sites are cleaned and lifted over to hg19 (UCSC chain) by scripts/build_fragile_sites.py; see cns/utils/fragile_sites.py for the processing details.

Licenses

Cite Adam Streck, Roland F Schwarz, CNSistent integration and feature extraction from somatic copy number profiles, GigaScience, Volume 14, 2025, giaf104. The code is available under the MIT License. The data and text files in the data and docs folders are available under the CC BY-NC 4.0 license.