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944 results

Bioinformatics

Publication
Nanopore long-read-only genome assembly of clinical Enterobacterales isolates is complete and accurate
February 27 2026
Publication
DUCKS4: a comprehensive workflow for nanopore sequencing analysis of facioscapulohumeral muscular dystrophy (FSHD)
February 6 2026
Publication
Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing
December 15 2025
Publication
Analysis of clinically relevant large tandem repeats using nanopore sequencing
December 4 2025
Publication
Targeted sequencing and iterative assembly of near-complete genomes
November 24 2025
Publication
Pre-phasing long reads improves structural variant genotyping
October 24 2025
Publication
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic
October 16 2025
Workflow
Workflow overview: 24-hour human whole-genome sequencing
September 17 2025
Getting started guide
Getting started guide: human genomics
September 17 2025
Publication
Nanopore- and AI-empowered microbial viability inference
September 3 2025
Case study
Case study: is the end to the diagnostic odyssey within reach?
August 27 2025
Case study
Case study: expanding reference genomes with T2T assembly to reflect global diversity
August 15 2025
Publication
DeepNanoHi-C: deep learning enables accurate single-cell nanopore long-read data analysis and 3D genome interpretation
July 10 2025
Publication
NANOME: a Nextflow pipeline for haplotype-aware allele-specific consensus DNA methylation detection by nanopore long-read sequencing
July 4 2025
Webinar
Uncovering gut prophage biology using long-read metagenomics
June 26 2025
Webinar
Long-read metagenomic sequencing and assembly of complex microbiomes using NanoMDBG
June 26 2025
Video
Exploring Oxford Nanopore sequencing methods for environmental samples
June 26 2025
Webinar
Clinical use of WGS: Cost-effective in-house approach
June 26 2025
Publication
Direct detection of 8-oxo-dG using nanopore sequencing
June 5 2025
Webinar
Integrative multiomics approaches in oncology and rare disease research
May 28 2025

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Nanopore long-read-only genome assembly of clinical Enterobacterales isolates is complete and accurate

DUCKS4: a comprehensive workflow for nanopore sequencing analysis of facioscapulohumeral muscular dystrophy (FSHD)

Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing

Analysis of clinically relevant large tandem repeats using nanopore sequencing

Targeted sequencing and iterative assembly of near-complete genomes

Pre-phasing long reads improves structural variant genotyping

Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic

Workflow overview: 24-hour human whole-genome sequencing

Getting started guide: human genomics

Nanopore- and AI-empowered microbial viability inference

Case study: is the end to the diagnostic odyssey within reach?

Case study: expanding reference genomes with T2T assembly to reflect global diversity

DeepNanoHi-C: deep learning enables accurate single-cell nanopore long-read data analysis and 3D genome interpretation

NANOME: a Nextflow pipeline for haplotype-aware allele-specific consensus DNA methylation detection by nanopore long-read sequencing

Uncovering gut prophage biology using long-read metagenomics

Long-read metagenomic sequencing and assembly of complex microbiomes using NanoMDBG

Exploring Oxford Nanopore sequencing methods for environmental samples

Clinical use of WGS: Cost-effective in-house approach

Direct detection of 8-oxo-dG using nanopore sequencing

Integrative multiomics approaches in oncology and rare disease research

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