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.
Multi-Omics Data for Target ID in Drug Discovery
How human genetics, single-cell transcriptomics, chromatin accessibility and proteomics combine into causal, cell-resolved target evidence, where integration usually fails, and how to grade the result before a programme is committed.
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Glasgow Computational Biology Community Event
Deep learning and agentic AI analysis of single-cell RNAseq data.
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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 scRNA-seq: A Complementary Pair
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 Marker Gene Identification Workflow 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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Best scRNA-seq Analysis Tools in 2026: Compared
Compare ScarfWeb, Loupe Browser, Trailmaker, Partek Flow, BBrowserX Pro, Omics Playground, Pluto Bio, and ROSALIND for scRNA-seq and multi-omics analysis in 2026.
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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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A guide to single-cell RNA sequencing analysis using web-based tools for non-bioinformatician
Sagnik Yarlagadda and Todd D. Giorgio provide a practical guide to scRNA-seq analysis using web-based platforms.
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Scarf enables a highly memory-efficient analysis of large-scale single-cell genomics data
Parashar Dhapola et al. introduce Scarf for memory-efficient single-cell sequencing analysis, published in Nature Communications.
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