The biology in your ligand-receptor analysis, and how to read it
Ligand-receptor analysis is easy to run and easy to over-read. How to get cell-cell communication biology from the ranked table, with LIANA and ScarfWeb.
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A curated index of articles, updates, events, and published work across single-cell research.
Integrating Multi-Omics Data for Effective Target Identification in Drug Discovery
Discover how multi-omics integration is reshaping drug discovery by uncovering disease mechanisms, prioritizing drug targets, and connecting genomics, epigenomics, transcriptomics, proteomics, and metabolomics into a usable biological model.
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Integrating Spatial Transcriptomics with Single-cell RNA-seq
How to integrate spatial transcriptomics with scRNA-seq: when spatial context helps, the key integration methods, and worked tissue examples.
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Spatial Transcriptomics and Single-cell RNA-seq: Complementary Technologies
The current state of spatial transcriptomics and scRNA-seq: single-cell-resolution platforms, foundation models for integration, spatial multi-omics, and 3D tissue atlases.
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When is Single-cell RNA-seq Enough, and When Do You Need Spatial Data?
When is scRNA-seq enough on its own? A guide to its use cases, the workflow from clustering to cell type annotation, and when to add spatial data.
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No-Code Workflow for Marker Gene Identification (Step-by-Step) in ScarfWeb
Find marker genes in scRNA-seq without code using ScarfWeb. Step-by-step walkthrough from upload and QC through clustering, marker detection, pseudotime, and export.
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Accelerate Marker Gene Detection in scRNA-seq: A No-Code Approach
Uncover the essentials of marker gene identification in single-cell RNA sequencing. This article covers no-code solutions, methodologies, and case studies across various fields.
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Designing Robust Single-Cell RNA-Seq Experiments: A Practical Guide
Learn the essentials of designing robust single-cell RNA-seq experiments with our practical guide for wet-lab scientists. Covers sample preparation, controls, sequencing parameters, and analysis approaches—including how no-code platforms eliminate computational barriers.
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A Practical Guide to Single-Cell RNA-Seq Cluster Annotation
How to annotate scRNA-seq clusters in 2026: marker genes, reference mapping, supervised tools, and separating cell identity from cell state.
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Building Cell Atlases - Navigating Biology Like Google Maps Navigates the World
Discover how building cell atlases parallels Google Maps - transforming scattered cellular data into integrated, navigable maps for drug discovery.
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Batch Effect Correction and Normalization in scRNA-Seq
Compare scRNA-seq normalization and batch correction methods, with current Seurat, Scanpy, Monocle 3, scran, Harmony, BBKNN and scVI workflows.
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Navigating the Complexity of Single-Cell RNA-Seq Data Analysis
Explore key challenges and advanced strategies in scRNA-seq data analysis for both new and experienced researchers.
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Overcoming Bioinformatics Skill Gaps in Single-Cell Research
Discover solutions to bridge bioinformatics skill gaps in single-cell research, enabling easier scRNA-seq analysis for wet-lab scientists.
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What is Single Cell Transcriptomics?
Discover single-cell transcriptomics, a transformative technique for analyzing gene expression at the cellular level in biology and medicine.
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