Resource Centre
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Multiomics whole-genome characterisation of a cancer genome using Oxford Nanopore sequencing
- Variant calling
- London Calling
- Cancer research
- Methylation
May 20 2025
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Pharmacogenomic Oxford Nanopore sequencing of the Twist Alliance Long-Read PGx Panel
- Variant calling
- Pharmacogenomics
- Biopharma
- Human genomics
- Clinical research
- Targeted
May 6 2025
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Workflow overview: human variant calling
- Variant calling
- Human genomics
- Clinical research
- Cancer research
- PromethION 24/48
- Whole genome
April 29 2025
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Flyer: methylation detection
- Variant calling
- Methylation
- Human genomics
- Cancer research
- Structural variation
- Clinical research
April 11 2025
Flyer: Hereditary Cancer Panel
- Variant calling
- Adaptive sampling
- Cancer research
- Clinical research
- Direct analysis
- DNA
April 11 2025
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ClairS-TO: a deep-learning method for long-read tumour-only somatic small variant calling
- Variant calling
- Cancer research
- Bioinformatics
- Q20+
- PromethION 24/48
- EPI2ME
March 13 2025
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Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
- Variant calling
- Targeted
- Human genomics
- Clinical research
- Long-read
- Structural variation
February 25 2025
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Getting started guide: single-cell transcriptomics
- Variant calling
- Single cell
- RNA
- cDNA
- Fusion transcript
- Transcriptome
February 24 2025
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Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes
- Variant calling
- Human genomics
- Clinical research
- PromethION 24/48
- Structural variation
- Methylation
January 3 2025
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Nanopore sequencing as a novel method of characterising anorexia nervosa risk loci
- Variant calling
- Human genomics
- Neuroscience
- Metabolic
- Targeted
- Adaptive sampling
December 31 2024
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Genewise detection of variants in MEFV gene using nanopore sequencing
- Variant calling
- Human genomics
- Amplicons
- MinION Mk1B
- Flongle
November 29 2024
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Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
- Variant calling
- Human genomics
- PromethION
- MinKNOW
- SNVs
November 4 2024
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Benchmarking reveals superiority of deep learning variant callers on bacterial nanopore sequence data
- Variant calling
- Microbiology
- Bacteria
- Whole genome
- MinION
- GridION
October 10 2024
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High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalogue of human genetic variation
- Variant calling
- Human genomics
- PromethION
- Methylation
- Structural variation
- Whole genome
October 2 2024
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Long-read whole-genome sequencing-based concurrent haplotyping and aneuploidy profiling of single cells
- Variant calling
- Bioinformatics
- Single cell
- Phasing
- PromethION
September 25 2024
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NCM 2024 technology update
- Variant calling
- Nanopore Community Meeting
- Bioinformatics
- Methylation
- Transcriptomics
- Whole genome
September 16 2024
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DeepSomatic: accurate somatic small variant discovery for multiple sequencing technologies
- Variant calling
- Bioinformatics
- Cancer research
- Phasing
August 19 2024
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Unlocking the banana pangenome: harnessing genetic diversity
- Variant calling
- Plant
- Population genomics
- Phasing
- Assembly
- Bioinformatics
May 24 2024
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Towards personalised medicine for breast cancer in the Caribbean: a pilot study
- Variant calling
- Cancer research
- Population genomics
- PromethION
- EPI2ME
- London Calling
May 24 2024
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Targeted sequencing of the entire blood group genome by adaptive sampling
- Variant calling
- Phasing
- Immunology
- London Calling
May 24 2024