scTCA: a hybrid Transformer-CNN architecture for imputation and denoising of scDNA-seq data

Single-cell DNA sequencing (scDNA-seq) has been widely used to unmask tumor copy number alterations (CNAs) at single-cell resolution. Despite that arm-level CNAs can be accurately detected from single-cell read counts, it is difficult to precisely identify focal CNAs as the read counts are featured with high dimensionality, high sparsity and low signal-to-noise ratio. This gives rise to a desperate demand for reconstructing high-quality scDNA-seq data. We develop a new method called scTCA for imputation and denoising of single-cell read counts, thus aiding in downstream analysis of both arm-level and focal CNAs. scTCA employs hybrid Transformer-CNN architectures to identify local and non-local correlations between genes for precise recovery of the read counts. Unlike conventional Transformers, the Transformer block in scTCA is a two-stage attention module containing a stepwise self-attention layer and a window Transformer, and can efficiently deal with the high-dimensional read counts data. We showcase the superior performance of scTCA through comparison with the state-of-the-arts on both synthetic and real datasets. The results indicate it is highly effective in imputation and denoising of scDNA-seq data.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2024-09-23
DOI
https://doi.org/10.1093/bib/bbae577
Citations
1
Primary Topic
Gene expression and cancer classification
Type
article
Field-Weighted Citation Impact
0.23

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article

scTCA: a hybrid Transformer-CNN architecture for imputation and denoising of scDNA-seq data

Zhenhua Yu, Furui Liu, Yang Li
1 citations
Briefings in Bioinformatics
Gene expression and cancer classification
0.23
article

scTCA: a hybrid Transformer-CNN architecture for imputation and denoising of scDNA-seq data

Zhenhua Yu, Furui Liu, Yang Li
article en
1 citations

Abstract

Single-cell DNA sequencing (scDNA-seq) has been widely used to unmask tumor copy number alterations (CNAs) at single-cell resolution. Despite that arm-level CNAs can be accurately detected from single-cell read counts, it is difficult to precisely identify focal CNAs as the read counts are featured with high dimensionality, high sparsity and low signal-to-noise ratio. This gives rise to a desperate demand for reconstructing high-quality scDNA-seq data. We develop a new method called scTCA for imputation and denoising of single-cell read counts, thus aiding in downstream analysis of both arm-level and focal CNAs. scTCA employs hybrid Transformer-CNN architectures to identify local and non-local correlations between genes for precise recovery of the read counts. Unlike conventional Transformers, the Transformer block in scTCA is a two-stage attention module containing a stepwise self-attention layer and a window Transformer, and can efficiently deal with the high-dimensional read counts data. We showcase the superior performance of scTCA through comparison with the state-of-the-arts on both synthetic and real datasets. The results indicate it is highly effective in imputation and denoising of scDNA-seq data.

Briefings in BioinformaticsVol. 25(6)
Ningxia University (CN)
Natural Science Foundation of Ningxia Province, Key Research and Development Program of Ningxia
Openalex Percentile: Top 41%
Gene expression and cancer classification
0.23
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