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DNA

Workflow
Workflow overview: NO-MISS
April 16 2026
Getting started guide
Getting started guide: microbial sequencing
February 20 2026
Workflow
Workflow overview: Hereditary Cancer Panel
January 20 2026
Publication
Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy
January 16 2026
Publication
Twist-ONT: combining nanopore sequencing with the Twist comprehensive viral research panel
January 7 2026
Publication
CRISPR-Cas9-induced double-strand breaks disrupt maintenance of epigenetic information
December 3 2025
Publication
Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing
November 3 2025
Poster
A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
October 14 2025
Publication
Decoding the Peruvian Amazon with in situ DNA barcoding of vertebrate and plant taxa
October 1 2025
Workflow
Workflow overview: amplicon sequencing
September 15 2025
Publication
Identification of non-coding causative variant underlying Warsaw Breakage syndrome using long-read based genomic sequencing and transcriptome analysis
September 12 2025
Publication
Long-read single-cell genome, transcriptome and open chromatin profiling links genotype to phenotypes
September 9 2025
Workflow
Workflow overview: direct RNA sequencing
September 8 2025
Publication
Swine influenza-modified pulmonary microbiota
September 8 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
Case study
Case study: unravelling tumour biology with single-cell Oxford Nanopore sequencing
August 8 2025
Case study
Case study: exploring the future of rapid leukaemia diagnosis with a single-platform workflow
August 7 2025
White paper
White paper: RNA and cDNA sequencing
July 31 2025

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Resource Centre

Workflow overview: NO-MISS

Getting started guide: microbial sequencing

Workflow overview: Hereditary Cancer Panel

Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy

Twist-ONT: combining nanopore sequencing with the Twist comprehensive viral research panel

CRISPR-Cas9-induced double-strand breaks disrupt maintenance of epigenetic information

Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing

A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing

​ Decoding the Peruvian Amazon with in situ DNA barcoding of vertebrate and plant taxa

Workflow overview: amplicon sequencing

Identification of non-coding causative variant underlying Warsaw Breakage syndrome using long-read based genomic sequencing and transcriptome analysis

Long-read single-cell genome, transcriptome and open chromatin profiling links genotype to phenotypes

Workflow overview: direct RNA sequencing

Swine influenza-modified pulmonary microbiota

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

Case study: unravelling tumour biology with single-cell Oxford Nanopore sequencing

Case study: exploring the future of rapid leukaemia diagnosis with a single-platform workflow

White paper: RNA and cDNA sequencing

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