Resource Centre
Bioinformatics tool )
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
Workflow )
Workflow overview: tumour-normal sequencing
Workflow )
Workflow overview: 24-hour human whole-genome sequencing
Workflow )
Workflow overview: plant genome assembly
Workflow )
Workflow overview: human variant calling
Workflow )
Workflow overview: direct RNA sequencing
Publication )
Whole human genome 5'-mC methylation analysis using long read nanopore sequencing
Video )
Whole-genome insights: nanopore sequencing in neuropathology
Video )
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
Video )
Resolving complex genomic structures and regulation patterns in cervical cancer
Video )
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
Video )
Investigating epigenomic alterations in cancer with nanopore sequencing
Company news )
"...we need a better name than follow through"
Company news )
"...a wafer thin update"
Publication )
In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia
Knowledge exchange )
Directly detect and phase genomic methylation with high reproducibility and low bias
Video )
Epigenetic patterns in a complete human genome
Video )
Using Oxford Nanopore sequencing in grapevine breeding
Publication )
Using long-read sequencing to detect imprinted DNA methylation
Video )
Untangling heterogeneity in DNA replication with nanopore sequencing
