Resource Centre
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Democratising Genomic Diagnostics: A New Model for Global Childhood Cancer Care
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Building sustainable pathogen genomic surveillance across Africa
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Welcome to London Calling 2026 | LC26
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Utility of long-read whole-genome sequencing across diverse clinical genomic investigations: a single- center experience | LC26
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Unlocking isoform programs underlying brain development with long-read single-cell RNA sequencing | LC26
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Understanding the role of rRNA modifications in colorectal cancer | LC26
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Understanding population-scale structural variation using long-read genomics | LC26
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Ultra-rapid genomic profiling of pediatric brain tumors using whole-genome and targeted long-read sequencing | LC26
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Translating long-read sequencing into a scalable NHS bioinformatics workflow | LC26
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Third-generation homozygosity analysis | LC26
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Targeted nanopore sequencing for newborn screening in a small population | LC26
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Targeted nanopore sequencing and an integrated analysis framework for neurogenomic disease | LC26
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Structural variant discovery in MENA individuals using Oxford Nanopore technology reveals clinically relevant variation | LC26
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Squiggles to the rescue: metagenomics-based pathogen surveillance | LC26
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Sharpening the hospital infection control toolset with front-line Oxford Nanopore sequencing | LC26
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RRR2 rapid respiratory response in rural and remote regions | LC26
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Revealing minor subpopulations in mixed infections with targeted sequencing | LC26
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Reconstruction of chromosome-scale copy number profiles of tumor genomes with long-read sequencing | LC26
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Real-time nanopore methylation and genomic profiling for pediatric cancer | LC26
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Rapid diagnosis of common, undetected, and uncultivable bloodstream infections from routine positive blood cultures | LC26
