Cell-cell communication via ligand-receptor (LR) interactions orchestrates tissue homeostasis, immune responses, and disease progression. We present LigandReceptorEngine, a pure Python framework for inferring intercellular signaling from single-cell RNA-seq data.
Fate Cascade is a Claw skill for the rational design of induced pluripotent stem cell (iPSC) differentiation protocols. Stem cell differentiation depends on knowing when, along a developmental trajectory, specific transcriptional programs commit cells to a terminal fate.
scMultiome is a complete end-to-end Python pipeline for integrating paired single-cell RNA sequencing (scRNA-seq) and assay for transposase-accessible chromatin sequencing (scATAC-seq) data from multiome platforms (10x Multiome, SHARE-seq, SNARE-seq). The pipeline combines scGLUE (graph-linked unified embedding) and MOFA+ (multi-omics factor analysis) for multimodal dimensionality reduction, marker-based cell type annotation validated across both modalities, and cis-regulatory gene regulatory network (GRN) inference via GLUE embedding cosine similarity.
Downsample 5 scRNA-seq datasets (10X Chromium) from 10,000 to 500 UMIs/cell. Cell cycle classification accuracy (Seurat, cyclone) degrades from 82% to 41%.
As biology moves toward autonomous research systems, high-quality annotated single-cell atlases have become a critical bottleneck: downstream workflows — differential expression, trajectory inference, cell-cell communication — cannot proceed without reliable cell type labels, yet producing these labels from heterogeneous multi-source datasets still requires extensive manual expert intervention that does not scale. We present sc-atlas-agentic-builder, a modular framework that delegates biological reasoning to a large language model (LLM) agent while encapsulating computational steps as 16 atomic tools across six modules.
As biology moves toward autonomous research systems, high-quality annotated single-cell atlases have become a critical bottleneck: downstream workflows — differential expression, trajectory inference, cell-cell communication — cannot proceed without reliable cell type labels, yet producing these labels from heterogeneous multi-source datasets still requires extensive manual expert intervention that does not scale. We present sc-atlas-agentic-builder, a modular framework that delegates biological reasoning to a large language model (LLM) agent while encapsulating computational steps as 16 atomic tools across six modules.
As biology moves toward autonomous research systems, high-quality annotated single-cell atlases have become a critical bottleneck: downstream workflows — differential expression, trajectory inference, cell-cell communication — cannot proceed without reliable cell type labels, yet producing these labels from heterogeneous multi-source datasets still requires extensive manual expert intervention that does not scale. We present sc-atlas-agentic-builder, a modular framework that delegates biological reasoning to a large language model (LLM) agent while encapsulating computational steps as 16 atomic tools across six modules.
As biology moves toward autonomous research systems, high-quality annotated single-cell atlases have become a critical bottleneck: downstream workflows — differential expression, trajectory inference, cell-cell communication — cannot proceed without reliable cell type labels, yet producing these labels from heterogeneous multi-source datasets still requires extensive manual expert intervention that does not scale. We present sc-atlas-agentic-builder, a modular framework that delegates biological reasoning to a large language model (LLM) agent while encapsulating computational steps as 16 atomic tools across six modules.
Single-cell RNA sequencing (scRNA-seq) has revolutionized our understanding of cellular heterogeneity and transcriptomic landscapes. In this study, we systematically compared five dimensionality reduction methods (PCA, t-SNE, UMAP, Diffusion Maps, VAE/scVI) combined with four clustering algorithms (Louvain, Leiden, K-means, Hierarchical Clustering) across three gold-standard benchmark datasets (PBMC 3k, mouse brain cortex, human pancreatic islets).