TY - JOUR
T1 - Cross-dataset pan-cancer detection by correlating cell-free DNA fragment coverage with open chromatin sites across cell types
AU - Olsen, Ludvig Renbo
AU - Odinokov, Denis
AU - Holsting, Jakob Qvortrup
AU - Kondrup, Karoline
AU - Iisager, Laura
AU - Rusan, Maria
AU - Buus, Simon
AU - Laursen, Britt Elmedal
AU - Borre, Michael
AU - Jochumsen, Mads Ryø
AU - Bouchelouche, Kirsten
AU - Frydendahl, Amanda
AU - Rasmussen, Mads Heilskov
AU - Henriksen, Tenna Vesterman
AU - Nesic, Marijana
AU - Demuth, Christina
AU - Lindskrog, Sia Viborg
AU - Nordentoft, Iver
AU - Lamy, Philippe
AU - Therkildsen, Christina
AU - Dyrskjøt, Lars
AU - Sørensen, Karina Dalsgaard
AU - Andersen, Claus Lindbjerg
AU - Jakobsen Skanderup, Anders
AU - Besenbacher, Søren
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - The fragmentation patterns of whole genome sequenced cell-free DNA are promising features for tumor-agnostic cancer detection. However, systematic biases challenge their cross-cohort generalization. We introduce LIONHEART, an open source cancer detection method specifically optimized to generalize across datasets. The method correlates bias-corrected cfDNA fragment coverage across the genome with the locations of accessible chromatin regions from 898 cell and tissue type features. We use these correlations to detect changes in the cell-free DNA cell type composition caused by cancer. We test LIONHEART on nine datasets and fourteen cancer types (1106 non-cancer controls, 1449 cancers) obtained from different studies and show that it can distinguish cancer samples from non-cancer controls across cohorts with ROC AUC scores ranging from 0.62-0.95 (mean = 0.83, std = 0.12). We further validate the method on an external dataset, achieving a ROC AUC of 0.917.
AB - The fragmentation patterns of whole genome sequenced cell-free DNA are promising features for tumor-agnostic cancer detection. However, systematic biases challenge their cross-cohort generalization. We introduce LIONHEART, an open source cancer detection method specifically optimized to generalize across datasets. The method correlates bias-corrected cfDNA fragment coverage across the genome with the locations of accessible chromatin regions from 898 cell and tissue type features. We use these correlations to detect changes in the cell-free DNA cell type composition caused by cancer. We test LIONHEART on nine datasets and fourteen cancer types (1106 non-cancer controls, 1449 cancers) obtained from different studies and show that it can distinguish cancer samples from non-cancer controls across cohorts with ROC AUC scores ranging from 0.62-0.95 (mean = 0.83, std = 0.12). We further validate the method on an external dataset, achieving a ROC AUC of 0.917.
UR - https://www.scopus.com/pages/publications/105026212594
U2 - 10.1038/s41467-025-66503-3
DO - 10.1038/s41467-025-66503-3
M3 - Journal article
C2 - 41271753
AN - SCOPUS:105026212594
SN - 2041-1722
VL - 16
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 11522
ER -