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Epigenetics

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: plant genome assembly
February 17 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
Video
Whole-genome insights: nanopore sequencing in neuropathology
May 19 2025
Video
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
November 18 2025
Video
Resolving complex genomic structures and regulation patterns in cervical cancer
April 11 2023
Video
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
June 26 2023
Video
Investigating epigenomic alterations in cancer with nanopore sequencing
October 11 2022
Company news
"...we need a better name than follow through"
December 1 2016
Company news
"...a wafer thin update"
September 29 2016
Publication
In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia
December 22 2020
Knowledge exchange
Directly detect and phase genomic methylation with high reproducibility and low bias
August 31 2021
Video
Epigenetic patterns in a complete human genome
November 17 2021
Video
Using Oxford Nanopore sequencing in grapevine breeding
May 24 2024
Publication
Using long-read sequencing to detect imprinted DNA methylation
February 22 2019
Video
Untangling heterogeneity in DNA replication with nanopore sequencing
May 29 2019

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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: plant genome assembly

Workflow overview: human variant calling

Workflow overview: direct RNA sequencing

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

Whole-genome insights: nanopore sequencing in neuropathology

Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing

Resolving complex genomic structures and regulation patterns in cervical cancer

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

Investigating epigenomic alterations in cancer with nanopore sequencing

"...we need a better name than follow through"

"...a wafer thin update"

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

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

Epigenetic patterns in a complete human genome

Using Oxford Nanopore sequencing in grapevine breeding

Using long-read sequencing to detect imprinted DNA methylation

Untangling heterogeneity in DNA replication with nanopore sequencing

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