Evidence map›Paper›PMID 39523623›Full record

ArticleBriefings in bioinformatics2024

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

Zhenhua Yu, Furui Liu, Yang Li

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Zhenhua YuSchool of Information Engineering, Ningxia University, 750021 Ningxia, China.ORCID 0000-0001-6526-6991
Furui LiuSchool of Information Engineering, Ningxia University, 750021 Ningxia, China.
Yang LiSchool of Information Engineering, Ningxia University, 750021 Ningxia, China.

Funding

Key Research and Development Program of Ningxia 2023BEG02009Natural Science Foundation of Ningxia Province 2023AAC05006
6 · The paper itself

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.

Indexed as

Single-Cell AnalysisAlgorithmsDNA Copy Number VariationsHigh-Throughput Nucleotide SequencingHumansNeural Networks, ComputerSequence Analysis, DNASignal-To-Noise RatioSoftwaredeep learningdenoisingimputationintra-tumor heterogeneitysingle-cell sequencingtransformer

Identifiers

PMID39523623
PMCPMC11551055

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.