Long non-coding RNAs (lncRNAs) are important regulators of cellular processes, but their analysis at single-cell resolution remains challenging because lncRNA prediction, quantification, cell-type-specific characterization and downstream functional interpretation are often performed using separate tools. Although single-cell RNA sequencing (scRNA-seq) and single-nucleus RNA sequencing (snRNA-seq) provide cellular-resolution transcriptomic profiles, reproducible workflows for lncRNA-focused analysis, particularly in plant systems, remain limited. To address this need, we developed scLncR, an open-source, modular and reproducible framework for lncRNA analysis in single-cell and single-nucleus transcriptomic data.
Methods
scLncR is a versatile framework incorporating multiple functional modules: lncRNA prediction, independent expression matrix processing, cell-type specific expression analysis, snRNA-seq/scRNA-seq expression enrichment analysis, weighted gene co-expression network analysis (WGCNA), pseudotime trajectory, and functional enrichment. It supports both command-line operation (for server-based customization) and a Shiny-based graphical user interface for user-friendly access.
Results
By connecting discrete analytical steps, scLncR enables a seamless transition from candidate lncRNA discovery to biological interpretation. Benchmarking revealed that our independent lncRNA matrix processing strategy enhances lncRNA signal visibility while preserving high concordance with established preprocessing methods at both cell-type and cluster levels. Notably, application to Arabidopsis root datasets prioritized three lncRNA candidates linked to root-hair cellular states and distinct genetic contexts.
Conclusions
scLncR serves as an open-source workflow resource designed to systematize and streamline lncRNA-focused analyses for single-cell and single-nucleus transcriptomic data. The source code, configuration files and documentation available at https://github.com/Lilab-SNNU/scLncR, release v1.0.0.
Bulk RNA-seq and single-cell RNA-seq (scRNA-seq) are widely used to investigate gene-expression changes, but downstream analysis often requires multiple statistical, visualization, and reporting tools, creating fragmented workflows that are difficult to configure and reproduce. We developed CoTRA (Comprehensive Toolbox...
An lncRNA-aware single-cell analysis framework — retaining all detectable GENCODE v45 lncRNAs during highly variable gene selection — combined with donor-level validation that guards against pseudoreplication is presented, and the pseudotime screen is reported as a negative result.
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PlantNetX integrates gene co-expression networks with cell-type expression, enabling fast identification and biological interpretation of candidate genes across tissues and individual cells, and will support research in plant cell-wall biosynthesis, pathway discovery, functional genomics, and crop improvement.
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NextLongIso is presented, a scalable and reproducible Nextflow pipeline that enables coordinated analysis of multiple layers of transcript regulation and facilitates the transition from transcript identification to functional interpretation of transcriptomic variation.
Cell-to-cell transcriptional heterogeneity, or noise, is an intrinsic property of the transcriptome with implications for development, disease progression, and aging. Bulk RNA-seq masks this variability by averaging gene expression across cells, whereas single-cell RNA sequencing (scRNA-seq) resolves it. Nevertheless,...
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