SigFormer: an Attention-Based Framework for Robust Single-Sample Mutational Signature Decomposition
Zhang, Y.; Niu, M.; Zong, C.
Show abstract
Somatic mutational signatures imprint the history of exogenous exposures and endogenous processes on the genome, offering critical insights into pathologic etiology and disease risk. However, accurate signature decomposition at the single-sample level is still challenging when mutation burden is low, sampling noise is high, and candidate catalogs are large and redundant. Here, we present SigFormer, a set-conditioned transformer framework designed to facilitate robust somatic mutation analysis without reliance on large cohorts. By leveraging a cross-attention mechanism between customized reference input and sample mutation profile, SigFormer improves exposure recovery and detection accuracy compared with likelihood-driven refitting (MuSiCal) with the largest performance gains in high-noise and overcomplete settings. On PCAWG genomes, SigFormer preserves major tissue-level structure while sensitively and accurately capturing cooccurrence of low-abundance signatures but without the need for tumor-type-specific gating. In low-burden normal-tissue datasets spanning clonal expansion and microdissection studies, SigFormer maintains the high accuracy and recovers stable tissue-dependent patterns of SBS1/SBS5/SBS40a, pointing to underlying tissue-specific mutagenic heterogeneity in normal tissues. Finally, SigFormer quantifies an explicit unattributable residual component when the catalogue is incomplete, preventing forced allocation into flexible flat signatures and providing a useful signal for downstream analyses.
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Dictionary learning for integrative, multimodal, and scalable single-cell analysis 97%
- Quantitative single cell 5hmC sequencing reveals non-canonical gene regulation by non-CG hydroxymethylation 96%
- Multi-omics integration and regulatory inference for unpaired single-cell data with a graph-linked unified embedding framework 96%
Similar papers in this journal
- Integrative, high-resolution analysis of single cell gene expression across experimental conditions with PARAFAC2-RISE 96%
- Multiome Perturb-seq unlocks scalable discovery of integrated perturbation effects on the transcriptome and epigenome 95%
- Iterative deep learning-design of human enhancers exploits condensed sequence grammar to achieve cell type-specificity 95%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.