Document repository

3914 个结果

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Webinar

Decoding complex disease through multiomics

In this webinar, our expert speakers will discuss how multiomic Oxford Nanopore sequencing supports a deeper understanding of disease mechanisms, by integrating DNA, RNA, and epigenetic analysis — all on a ...

July 22, 2026

Publication

The planktonic microbiome of the Great Barrier Reef

Authors: Steven Robbins, Marko Terzin, Katherine Dougan, Julian Zaugg, Sara C. Bell, Patrick W. Laffy, J. Pamela Engelberts, Kim-Anh Lê Cao, Renee K. Gruber, Nicole S. Webster, David G ...

July 22, 2026

Publication

From culture to clarity in four hours: accelerating clinical management of bloodstream infections using metagenomics

Authors: Jawad Ali, Anurag Basavaraj Bellankimath, Silje Therese Opgård, Emil Varman Manivannan, Gunnar Skov Simonsen, Rafi Ahmad

July 20, 2026

Application note

Application note: library preparation using the Ligation Sequencing Kit XL V14 from Oxford Nanopore Technologies on epMotion

In this application note, explore how the Oxford Nanopore Ligation Sequencing Kit XL V14 can be seamlessly automated on the Eppendorf epMotion systems.

July 15, 2026

Application note

Application note: library preparation using epMotion and Oxford Nanopore Technologies Native Barcoding Kit 96 V14

In this application note, discover an automated solution for preparing up to 96 sequencing libraries with the Oxford Nanopore Native Barcoding Kit 96 V14 on the Eppendorf epMotion systems.

July 15, 2026

Case study

Case study: cell-free DNA sequencing and methylation detection — promising potential for non-invasive cancer monitoring

In this case study, find out how researchers are using nanopore technology to analyse cfDNA for cancer monitoring.

July 14, 2026

Workflow overview

Workflow overview: direct RNA sequencing

This end-to-end workflow provides a simple method to characterise RNA modifications from a human blood research sample using direct RNA sequencing.

July 9, 2026

Workflow overview

Workflow overview: bulk transcriptomics

This end-to-end workflow provides a flexible method to sequence full-length transcripts for isoform-level expression analysis.

July 9, 2026

Publication

Nanopore metagenomic sequencing links clinically relevant resistance determinants to pathogens

Authors: Harika Ürel, Ela Sauerborn, Michael Biggel, Friedemann Gebhardt, Ebenezer Foster-Nyarko, Silvio D Brugger, Rhys T White, Søren Heidelbach, Mads Albertsen, Francis Muchaamba, Tim Reska, Marc J A Stevens ...

July 8, 2026

Publication

Beyond bisulfite sequencing: resolving 5-hmC with nanopore sequencing unmasks the true-5mC methylation entropy landscape

Authors: Uri Bertocchi, Eyal Katz, Jonathan Jeffet, Assaf Grunwald, Neiv Gabay, Jasline Deek, Sujal Verma, Amit Shwartz, Gali Umschweif–Nevo, Bernard Lerer, Yael Roichman, Yuval Ebenstein

July 8, 2026

Publication

Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathies

Authors: Dennis Yeow, Andre L. M. Reis, Igor Stevanovski, et al.

July 4, 2026

Publication

Long-read sequencing maps transposable element variation and its regulatory and epigenetic effects in the human brain

Authors: Alexis Ayuketah, Melissa Meredith, Cristian Groza, et al.

July 3, 2026

Publication

Hierarchical classification of haematologic malignancies using epigenetic and genetic information

Authors: Maximilian Schönung, Melissa Türe, Panna Lajer, et al.

July 3, 2026

Getting started guide

Getting started guide: bulk transcriptomics

This guide introduces cDNA and direct RNA Oxford Nanopore sequencing, for ultra-rich transcriptomic data without compromise.

July 3, 2026

Case study

Case study: large-cohort cDNA sequencing advances multiomic insights into neurodegenerative disease

In this case study, discover how Kimberley Billingsley and her colleagues at the National Institutes of Health are using Oxford Nanopore large-cohort cDNA sequencing to research the human brain ...

July 3, 2026

Publication

Performance and practicality of 16S nanopore sequencing for routine bacterial identification in clinical samples

Authors: A.U. Geers, C. Bütikofer, M. A. Terrazos Miani, S. Droz, A. Zihler Berner, I. Lendenmann, C. Hirzel, P.M. Keller, F. Suter-Riniker, S. Neuenschwander, C. Casanova, A ...

July 2, 2026

Publication

Epigenetic liquid biopsy enables universal mutation-agnostic molecular surveillance for high-risk neuroblastoma

Publication: Epigenetic liquid biopsy enables universal mutation-agnostic molecular surveillance for high-risk neuroblastoma

July 1, 2026

Publication

Intact and single-molecule analysis of heparan sulfate

Publication: Intact and single-molecule analysis of heparan sulfate

June 29, 2026

Publication

Comparison of nanopore sequencing, Methylation EPIC array, and EM-Seq for DNA methylation detection

Publication: Comparison of nanopore sequencing, Methylation EPIC array, and EM-Seq for DNA methylation detection

June 25, 2026

Publication

Female-specific m6A remodelling in the liver correlates with post transcriptional metabolic adaptation to high fat diet

Publication: Female-specific m6A remodelling in the liver correlates with post transcriptional metabolic adaptation to high fat diet

June 22, 2026

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Document repository

Decoding complex disease through multiomics

The planktonic microbiome of the Great Barrier Reef

From culture to clarity in four hours: accelerating clinical management of bloodstream infections using metagenomics

Application note: library preparation using the Ligation Sequencing Kit XL V14 from Oxford Nanopore Technologies on epMotion

Application note: library preparation using epMotion and Oxford Nanopore Technologies Native Barcoding Kit 96 V14

Case study: cell-free DNA sequencing and methylation detection — promising potential for non-invasive cancer monitoring

Workflow overview: direct RNA sequencing

Workflow overview: bulk transcriptomics

Nanopore metagenomic sequencing links clinically relevant resistance determinants to pathogens

Beyond bisulfite sequencing: resolving 5-hmC with nanopore sequencing unmasks the true-5mC methylation entropy landscape

Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathies

Long-read sequencing maps transposable element variation and its regulatory and epigenetic effects in the human brain

Hierarchical classification of haematologic malignancies using epigenetic and genetic information

Getting started guide: bulk transcriptomics

Case study: large-cohort cDNA sequencing advances multiomic insights into neurodegenerative disease

Performance and practicality of 16S nanopore sequencing for routine bacterial identification in clinical samples

Epigenetic liquid biopsy enables universal mutation-agnostic molecular surveillance for high-risk neuroblastoma

Intact and single-molecule analysis of heparan sulfate

Comparison of nanopore sequencing, Methylation EPIC array, and EM-Seq for DNA methylation detection

Female-specific m6A remodelling in the liver correlates with post transcriptional metabolic adaptation to high fat diet

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