Resource Centre
Workflow )
Workflow overview: tumour-normal sequencing
Workflow )
Workflow overview: single-cell transcriptomics
Workflow )
Workflow overview: 24-hour human whole-genome sequencing
Workflow )
Workflow overview: plant genome assembly
Workflow )
Workflow overview: human variant calling
Video )
Whole-genome insights: nanopore sequencing in neuropathology
Video )
Variant phasing for antisense oligonucleotide design using adaptive sampling
Publication )
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
Video )
Utilizing nanopore long-read sequencing to simplify hereditary movement disorder diagnostics
Video )
Ultra-fast deep-learned classification algorithms for diagnosing pediatric CNS and solid tumors
Publication )
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
Video )
Towards routine modopathy diagnostics: advances and clinical application of direct RNA sequencing
Publication )
The mutational and clonality profile of HGSOC is established early in tumour development and conserved throughout therapy resistance
Publication The implementation of genome sequencing in rare genetic diseases diagnosis: a pilot study from the Hong Kong genome project
Publication )
The correlation between CpG methylation and gene expression is driven by sequence variants
Publication )
Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
Publication )
A systematic benchmark of nanopore long-read RNA sequencing for transcript-level analysis in human cell lines
Publication )
Structural patterns and transcriptional effects of integrated Epstein-Barr virus revealed by long-read sequencing and RNA-sequencing in NPC
Publication )
Singleton rapid long-read genome sequencing as first-tier genetic test for critically ill children with suspected genetic diseases
Publication )
Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling
