Single-cell RNA sequencing has enabled the construction of comprehensive cell atlases, yet the quality and coherence of the cell-type annotations within these atlases remain largely unexamined. When a label is applied to a transcriptionally heterogeneous population, the downstream analyses that depend on it, and automated label transfer in particular, become unreliable. We present scINTILLA (Single-Cell Integrated Inference, Labelling, and Landscape Analysis), a computational framework that combines supervised and unsupervised machine learning to score the learnability and internal consistency of cell-type labels in single-cell datasets. The unsupervised arm benchmarks a broad panel of clustering algorithms and derives a neighbourhood confusion score for every cell, whilst the supervised arm trains up to twelve classifiers and extracts prediction agreement, entropy, and confidence. These signals are normalised and aggregated into a single composite score per cell type, where a low score flags label ambiguity or concealed heterogeneity. As a by-product, scIN-TILLA also reports which clustering and classification algorithms perform best on a given dataset, offering practical guidance for downstream label transfer. We applied it to five Human Cell Atlas datasets spanning the adult brain, lung, eye, and two organoid atlases, and recovered clear differences in the learnability and internal consistency of annotations across atlases that were not driven by the number of annotated cell types. Focused re-analysis of lowscoring populations in the lung and endoderm-organoid atlases resolved biologically coherent sub-populations, in some cases with context-specific enrichment, much of it recovered from cells that had been assigned broad or catch-all labels. scINTILLA is advisory rather than prescriptive, guiding principled, data-driven re-annotation at atlas scale.
Single-cell RNA sequencing fundamentally depends on defining cell–cell similarity to resolve distinct cell states. However, conventional dimensional-reduction frameworks such as t-SNE and UMAP inherently rely on Euclidean geometry, a construct ill-suited for high-dimensional, sparse count matrices, and produce cluster...
Henry Han, Tian-Yun Zhang, Lu-Yu Niu et al.· bioRxiv· 0 citations
The results indicate that GmGM provides a unified, reproducible framework for joint cell clustering and gene-network inference, capable of revealing cellular structure beyond that captured by conventional pipelines.
O. Lanzetta, L. Cutillo, Bailey Andrew et al.· 0 citations
This Review systematically integrates current conceptual frameworks, computational methodologies, and domain-specific best practices for cell-type annotation in cardiovascular single-cell research and offers practical recommendations and discuss future directions encompassing multimodal integration, spatial transcripto...
Lu Sun, Li Ma, Li-Zhi Chen et al.· International Journal of Bio...· 0 citations
CARA is introduced, a cross-omics Bayesian framework that transfers cell type knowledge from scRNA-seq to scATAC-seq and detects novel cell types in single-cell DNA methylation data, demonstrating seamless extensibility to new modalities.
Lan Cao, Wenhao Zhang, Feng Zhou et al.· Genome Research· 0 citations
NetMap is presented, a pipeline that jointly infers cell-level GRNs and clusters cells based on shared regulatory programs, combining state-of-the-art single-cell autoencoders and explainable artificial intelligence methods that outperforms existing methods on synthetic data with a known ground-truth GRN and is able to...
A. Hartebrodt, Mhaned Oubounyt, G. D. de Almeida et al.· bioRxiv· 0 citations
A cell-by-gene count matrix is the artifact of a single-cell RNA-seq experiment that is most often stored, shared, and reanalyzed. It is the output of a computation whose inputs are the sequenced molecules and a gene annotation, and while the molecules never change, the annotation is revised continually. Once the matri...
R. Patro· bioRxiv· 0 citations
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