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325 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
Publication
Whole human genome 5'-mC methylation analysis using long read nanopore sequencing
May 21 2021
Poster
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
May 15 2023
Video
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
November 18 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
Publication
In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia
December 22 2020
Publication
Virtual Nanopore Day, Switzerland
November 25 2020
Video
Virtual Nanopore Day, Australia: Bioinformatics
November 25 2020
Knowledge exchange
Directly detect and phase genomic methylation with high reproducibility and low bias
August 31 2021
Publication
Using long-read sequencing to detect imprinted DNA methylation
February 22 2019
Poster
Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
May 15 2023
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
Publication
Publication: Ultra-fast deep-learned CNS tumour classification during surgery
October 11 2023

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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

Whole human genome 5'-mC methylation analysis using long read nanopore sequencing

Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation

Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing

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

Detecting, classifying, and monitoring CNS tumors with nanopore sequencing

In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia

Virtual Nanopore Day, Switzerland

Virtual Nanopore Day, Australia: Bioinformatics

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

Using long-read sequencing to detect imprinted DNA methylation

Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C

Uncovering hidden variation in rare and complex diseases webinar

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

Publication: Ultra-fast deep-learned CNS tumour classification during surgery

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