ArticleNature communications2024
scLENS: data-driven signal detection for unbiased scRNA-seq data analysis.
Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- scSpecies: enhancement of network architecture alignment in comparative single-cell studies.Genome biology · 2025Article
- scICE: enhancing clustering reliability and efficiency of scRNA-seq data with multi-cluster label consistency evaluation.Nature communications · 2025Article
- Principled PCA separates signal from noise in omics count data.bioRxiv : the preprint server for biology · 2025Article
- scLENS: data-driven signal detection for unbiased scRNA-seq data analysis.Nature communications · 2024Article
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Authors and funding
6 authors.
Funding
Abstract
High dimensionality and noise have limited the new biological insights that can be discovered in scRNA-seq data. While dimensionality reduction tools have been developed to extract biological signals from the data, they often require manual determination of signal dimension, introducing user bias. Furthermore, a common data preprocessing method, log normalization, can unintentionally distort signals in the data. Here, we develop scLENS, a dimensionality reduction tool that circumvents the long-standing issues of signal distortion and manual input. Specifically, we identify the primary cause of signal distortion during log normalization and effectively address it by uniformizing cell vector lengths with L2 normalization. Furthermore, we utilize random matrix theory-based noise filtering and a signal robustness test to enable data-driven determination of the threshold for signal dimensions. Our method outperforms 11 widely used dimensionality reduction tools and performs particularly well for challenging scRNA-seq datasets with high sparsity and variability. To facilitate the use of scLENS, we provide a user-friendly package that automates accurate signal detection of scRNA-seq data without manual time-consuming tuning.
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Registered trials
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