Resource Centre
Poster )
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
Poster )
Whole genome Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.
Poster )
Whole-genome DNA sequencing using nanopore R10.4 promises best practice for single-cell variation detection and methylation profiling
Poster )
Whole-genome analysis of VREfm isolates with daptomycin resistance using Oxford Nanopore and Illumina sequencing
Poster )
Validation and application of multiplex nanopore MinION sequencing for molecular typing of human adenoviruses in clinical samples: a cost effective sequencing strategy
Poster )
Validation and quality control of a molecular cloning experiment using de novo assembly of Oxford Nanopore reads
Poster )
Use of the Oxford Nanopore MinION sequencer for rapid MLST genotyping of streptococcus pneumoniae
Poster )
Unsupervised Barcode Demultiplexing
Poster )
Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
Poster )
Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing
Poster )
Unlocking Nanopore sequencing for managing food safety in the food industry
Poster )
Universal, amplicon-based sequencing method for Canine Morbillivirus (CDV)
Poster )
Understanding genetic variation in cancer using targeted long-read sequencing
Poster )
Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing
Poster )
Ultra-long reads and ultra-long duplications: What nanopore sequencing is revealing about Bordetella pertussis
Poster )
Ultra-fast deep-learned pediatric CNS tumor classification during surgery
Poster )
Ultra-fast and cost-effective pathogen identification and resistance gene detection in a clinical research setting using nanopore Flongle sequencing
Poster )
Translocation detection in cancer using low-pass pore-c sequencing
Poster Translocation and extrachromosomal DNA (ecDNA) detection in cancer using low-pass Pore-C sequencing
Poster )
Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
