Resource Centre
ZCWPW1 loss-of-function variants in Alzheimer’s Disease
- Clinical research
- Long-read
- Phasing
- Variant calling
- Human genomics
- Targeted
Workflow overview: single-cell transcriptomics
- Clinical research
- Single cell
- Transcriptome
- PromethION 24/48
- Cancer research
- cDNA
Workflow overview: pharmacogenomics with adaptive sampling
- Clinical research
- Pharmacogenomics
- Biopharma
- Human genomics
- Targeted
- Variant calling
Workflow overview: large cohort sequencing
- Clinical research
- Workflow
- Human genomics
- Population genomics
- Whole genome
- Structural variation
Workflow overview: human variant calling
- Clinical research
- Human genomics
- Cancer research
- PromethION 24/48
- Whole genome
- Variant calling
Workflow overview: direct RNA sequencing
- Clinical research
- Workflow
- RNA
- cDNA
- Methylation
- Epigenetics
Workflow overview: bacterial isolate sequencing
- Clinical research
- Bacteria
- Whole genome
- DNA
- Microbiology
- Infectious disease
The WIPE assay for selection and elimination of HIV-1 provirus in vitro using latency-reversing agents
- Clinical research
- Microbiology
- Virus
- MinION
- Whole genome
- RNA
Widespread occurrence of hybrid internal-terminal exons in human transcriptomes
- Clinical research
- Transcriptome
- Long-read
- RNA
- cDNA
- Isoforms
Whole genome sequencing reveals virulence potentials of Helicobacter pylori strain KE21 isolated from a Kenyan patient with gastric signet ring cell carcinoma
- Clinical research
- Microbiology
- Infectious disease
- Bacteria
- Cancer research
- MinION
Whole-genome sequencing of rare disease patients in a national healthcare system
- Clinical research
- Human genomics
- Whole genome
- DNA
- gDNA
- Structural variation
Whole-genome sequencing of human Enteroviruses from clinical samples by nanopore direct RNA sequencing
- Clinical research
- Microbiology
- Virus
- Whole genome
- Assembly
- Direct analysis
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
- Clinical research
- PromethION
- gDNA
- Whole genome
- Variant calling
- Structural variation
Whole genome sequencing and phylogenetic classification of Tunisian SARS-CoV-2 strains from patients of the Military Hospital in Tunis
- Clinical research
- Microbiology
- Infectious disease
- Virus
- Outbreak
- GridION
Whole-genome sequencing and genetic diversity of severe fever with thrombocytopenia syndrome virus using multiplex PCR-based nanopore sequencing, Republic of Korea
- Clinical research
- Virus
- Microbiology
- Long-read
- MinION
Whole-genome insights: nanopore sequencing in neuropathology
- Clinical research
- PromethION 2
- PromethION 24/48
- EPI2ME
- Epigenetics
- Fusion transcript
Whole genome assembly of human papillomavirus by nanopore long-read sequencing
- Clinical research
- Oncology
- Cancer research
- Microbiology
- Infectious disease
- MinION
Whole-genome analysis of VREfm isolates with daptomycin resistance using Oxford Nanopore and Illumina sequencing
- Clinical research
- Bioinformatics
- Whole genome
- Infectious disease
- Bacteria
- Microbiology
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
- Clinical research
- Cancer research
- Human genomics
- Phasing
- Methylation
- Epigenetics