Resource Centre
Poster 
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
Publication 
Comparison of structural variants detected by PacBio-CLR and ONT sequencing in pear
Poster 
Multi-component data types from single experiments can resolve complex imprinting-disorder mechanisms
Poster Clone-and haplotype-specific copy number variation inference in heterogeneous bulk tumour samples
Publication 
The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation
Publication 
Construction of a trio-based structural variation panel utilizing activated T lymphocytes and long-read sequencing technology
Publication 
Haplogenome assembly reveals interspecific structural variation in Eucalyptus hybrids
Publication 
Gapless assembly of complete human and plant chromosomes using only nanopore sequencing
Publication 
Reference genome assemblies reveal the origin and evolution of allohexaploid oat
Publication 
Transcriptomic complexity in strawberry fruit development and maturation revealed by nanopore sequencing
Publication 
De novo assembly of human genome at single-cell levels
Publication 
Frequent spontaneous structural rearrangements promote transgenerational genome diversification in Brassica napus
Publication 
A global regulatory network for dysregulated gene expression and abnormal metabolic signaling in immune cells in the microenvironment of Graves’ disease and Hashimoto’s thyroiditis
Publication 
Phasing analysis of lung cancer genomes using a long read sequencer
Publication 
Identifying synergistic high-order 3D chromatin conformations from genome-scale nanopore concatemer sequencing
Publication 
Complete sequences of six Major Histocompatibility Complex haplotypes, including all the major MHC class II structures
Publication 
Alternative splicing regulation of glycine-rich proteins via target of rapamycin-reactive oxygen species pathway in Arabidopsis seedlings upon glucose stress
Publication 
Detection of structural variations and fusion genes in breast cancer samples using third-generation sequencing
Publication 
Direct full-length RNA sequencing reveals an important role of epigenetics during sexual reversal in Chinese soft-shelled turtle
Publication 
Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue
