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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: large cohort sequencing
July 28 2025
Workflow
Workflow overview: human variant calling
April 29 2025
Workflow
Workflow overview: direct RNA sequencing
September 8 2025
Poster
Whole genome Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.
May 19 2023
Video
Whole-genome insights: nanopore sequencing in neuropathology
May 19 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
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
July 14 2023
Company news
"...we need a better name than follow through"
December 1 2016
Company news
"...a wafer thin update"
September 29 2016
Knowledge exchange
Directly detect and phase genomic methylation with high reproducibility and low bias
August 31 2021
Publication
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
June 25 2020
Video
Using Oxford Nanopore sequencing in grapevine breeding
May 24 2024
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
Video
Understanding the binding of multiple transcription factors by base-pair-resolution chromatin accessibility
September 17 2024

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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: large cohort sequencing

Workflow overview: human variant calling

Workflow overview: direct RNA sequencing

Whole genome Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.

Whole-genome insights: nanopore sequencing in neuropathology

Resolving complex genomic structures and regulation patterns in cervical cancer

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

Detecting, classifying, and monitoring CNS tumors with nanopore sequencing

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

"...a wafer thin update"

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

Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci

Using Oxford Nanopore sequencing in grapevine breeding

Using long-read sequencing to detect imprinted DNA methylation

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

Understanding the binding of multiple transcription factors by base-pair-resolution chromatin accessibility

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