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78 results

Methylation

Bioinformatics tool
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
June 16 2021
Workflow
Workflow overview: tumour-normal sequencing
July 21 2025
Workflow
Workflow overview: 24-hour human whole-genome sequencing
September 17 2025
Workflow
Workflow overview: large cohort sequencing
July 28 2025
Workflow
Workflow overview: human variant calling
April 29 2025
Workflow
Workflow overview: direct RNA sequencing
September 8 2025
Video
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
June 26 2023
Video
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
July 14 2023
Knowledge exchange
Directly detect and phase genomic methylation with high reproducibility and low bias
August 31 2021
Webinar
Uncovering hidden variation in rare and complex diseases webinar
August 7 2025
Publication
Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
January 30 2026
Bioinformatics tool
Towards inferring nanopore sequencing ionic currents from nucleotide chemical structures
December 2 2020
Publication
The correlation between CpG methylation and gene expression is driven by sequence variants
July 24 2024
Case study
Testimonial: Jonathan Mill
April 7 2025
Bioinformatics tool
Targeted nanopore sequencing by real-time mapping of raw electrical signal with UNCALLED
November 30 2020
Bioinformatics tool
Systematic benchmarking of tools for CpG methylation detection from Nanopore sequencing
October 15 2020
Video
Structural variant analysis with Oxford Nanopore
October 30 2020
Publication
A single fiber view of the nucleosome organization in eukaryotic chromatin
November 22 2023
Case study
Case study: simple, simultaneous detection of epigenetic and genetic variants for insights into disease mechanisms
February 13 2024
Bioinformatics tool
PycoMeth: A toolbox for differential methylation testing from nanopore methylation calls
February 19 2022

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Resource Centre

Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads

Workflow overview: tumour-normal sequencing

Workflow overview: 24-hour human whole-genome sequencing

Workflow overview: large cohort sequencing

Workflow overview: human variant calling

Workflow overview: direct RNA sequencing

Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants

Detecting, classifying, and monitoring CNS tumors with nanopore sequencing

Directly detect and phase genomic methylation with high reproducibility and low bias

Uncovering hidden variation in rare and complex diseases webinar

Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars

Towards inferring nanopore sequencing ionic currents from nucleotide chemical structures

The correlation between CpG methylation and gene expression is driven by sequence variants

Testimonial: Jonathan Mill

Targeted nanopore sequencing by real-time mapping of raw electrical signal with UNCALLED

Systematic benchmarking of tools for CpG methylation detection from Nanopore sequencing

Structural variant analysis with Oxford Nanopore

A single fiber view of the nucleosome organization in eukaryotic chromatin

Case study: simple, simultaneous detection of epigenetic and genetic variants for insights into disease mechanisms

PycoMeth: A toolbox for differential methylation testing from nanopore methylation calls

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