Search bioRxiv⌕ Search

bioRxiv · 10.1101/818062

CNLLRR: A Novel Low-Rank Representation Method for Single-cell RNA-seq Data Analysis

Abstract

The development of single-cell RNA-sequencing (scRNA-seq) technology has enabled the measurement of gene expression in individual cells. This provides an unprecedented opportunity to explore the biological mechanisms at the cellular level. However, existing scRNA-seq analysis methods are susceptible to noise and outliers or ignore the manifold structure inherent in the data. In this paper, a novel method called Cauchy non-negative Laplacian regularized low-rank representation (CNLLRR) is proposed to alleviate the above problem. Specifically, we employ the Cauchy loss function (CLF) instead of the conventional norm constraints in the noise matrix of CNLLRR, which will enhance the robustness of the method. In addition, graph regularization term is applied to the objective function, which can capture the paired geometric relationships between cells. Then, alternating direction method of multipliers (ADMM) is adopted to solve the optimization problem of CNLLRR. Finally, extensive experiments on scRNA-seq data reveal that the proposed CNLLRR method outperforms other state-of-the-art methods for cell clustering, cell visualization and prioritization of gene markers. CNLLRR contributes to understand the heterogeneity between cell populations in complex biological systems.\n\nAuthor summaryAnalysis of single-cell data can help to further study the heterogeneity and complexity of cell populations. The current analysis methods are mainly to learn the similarity between cells and cells. Then they use the clustering algorithm to perform cell clustering or downstream analysis on the obtained similarity matrix. Therefore, constructing accurate cell-to-cell similarity is crucial for single-cell data analysis. In this paper, we design a novel Cauchy non-negative Laplacian regularized low-rank representation (CNLLRR) method to get a better similarity matrix. Specifically, Cauchy loss function (CLF) constraint is applied to punish noise matrix, which will improve the robustness of CNLLRR to noise and outliers. Moreover, graph regularization term is applied to the objective function, which will effectively encode the local manifold information of the data. Further, these will guarantee the quality of the cell-to-cell similarity matrix learned. Finally, single-cell data analysis experiments show that our method is superior to other representative methods.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yu, N., Liu, J.-X., Gao, Y.-L., Zheng, C.-H., Shang, J., Cai, H.. 2019-10-24. CNLLRR: A Novel Low-Rank Representation Method for Single-cell RNA-seq Data Analysis. https://doi.org/10.1101/818062

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

StableProt: Structure-Aware Deep Learning for Protein Thermostability (Tm) and Environmental Adaptation (OGT) Prediction

Predicting protein melting temperature (Tm) and organismal optimal growth temperature (OGT) is essential for enzyme engineering, biocatalyst design, and metagenomic bioprospecting, yet computational prediction faces several fundamental bottlenecks: sequence-only representations miss tertiary packing; dual-task coupling induces destructive gradient conflict; natural database skew (>87% mesophiles) drives mesophilic collapse; and existing tools produce uncalibrated point predictions. To address these challenges, we present StableProt, a structure-aware framework that couples amino acid sequences with Foldseek 3Di structural tokens via a frozen SaProt backbone to capture 3D contacts. Disjoint heads condition thermodynamic stability on ecological context without gradient conflict, while targeted 14% mesophilic subsampling expands thermophile representation to eliminate mesophilic collapse. Calibrated ensemble modeling reduces calibration error to 1.92%, providing dependable 95% confidence intervals. Evaluating models across 10{degrees}C temperature intervals reveals severe baseline collapse at thermal extremes, whereas StableProt maintains robust accuracy across regimes. On ProThermDB and zero-shot FireProtDB, StableProt achieves state-of-the-art probabilistic accuracy (CRPS = 4.52{degrees}C and 8.71{degrees}C) while recovering 92.0% of hyperthermophiles ([≥]80{degrees}C), and in prospective validation, its calibrated intervals capture both enzyme stability (75.3% coverage) and host environmental growth temperatures (78.1% coverage). StableProt is freely accessible as an interactive web server at https://stableprot.dixitlab.org/.

bioinformatics↗

RoDPAA: A Robust Dissimilarity-Based Principal Angle Analysis Framework for Multi-View Microbiome Data Integration

Multiview microbiome studies profile the same participants across body sites or molecular layers, but integration is hampered by sparse, compositional data, modest sample sizes and methods that recognize only exact sharing. We present RoDPAA (Robust Dissimilarity-based Principal Angle Analysis), a framework that represents each view through any data-appropriate dissimilarity, such as Bray--Curtis, without log-ratio transformation or likelihood assumptions. RoDPAA aligns view-specific signal subspaces through principal angles, captures complete and partial sharing, and tests by permutation how many components are shared, using only eigendecomposition and little tuning. In Gaussian simulations, RoDPAA matched JIVE and MOFA given true ranks, ran faster and alone recovered the shared dimension in every replicate. In two inflammatory bowel disease (IBD) cohorts with sparse, zero-inflated data, Bray--Curtis-based RoDPAA recovered shared structure that was stable to prevalence filtering, whereas log-ratio-based alternatives were not. Its leading microbiome--metabolome factors, learned without disease labels, were the only ones associated with IBD.

bioinformatics↗

Deducing splicing events from transcript sets with splicelogic

Long-read RNA sequencing captures a greater proportion of full-length transcripts, enabling more accurate isoform identification, discovery of novel isoforms, and more precise differential transcript usage analysis. However, comparing transcripts, whether between conditions or between sets such as novel and annotated isoforms, yields complex isoform changes that are hard to manipulate, summarize, and visualize. This is compounded by vertical integration of some tools, where downstream analysis depends on the specific output of a particular upstream tool. To address this gap, we have developed splicelogic, an R/Bioconductor package that makes transcript-set comparisons biologically interpretable by turning them into discrete splicing events, such as exon skipping, alternative splice sites, intron retention, and alternative transcription start and end sites. We designed splicelogic to integrate easily with existing RNA-seq workflows and tools. The splicelogic functions are modular, readable, and extensible, making it easy for users to adapt core logic to their own custom scientific questions or novel splicing definitions. By obtaining interpretable splicing events from transcript changes, splicelogic enables downstream analyses, including annotation of RNA-binding protein recognition sites, alongside summary statistics and visualization. The splicelogic package is publicly available and distributed through Bioconductor.

bioinformatics↗