April 16, 2019 article Open access Multi-platform discovery of haplotype-resolved structural variation in human genomes Nature Communications DOI: 10.1038/s41467-018-08148-z Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 12 stored of 1,055 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access Comparison and benchmark of structural variants detected from long read and long-read assembly 2023 Briefings in Bioinformatics article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 15 citations Chromosomal breaks at the origin of small tandem DNA duplications 2022 BioEssays review Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 3 citations SVision: a deep learning approach to resolve complex structural variants 2022 Nature Methods article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access cited by 1 patent 119 citations Comparison and benchmark of long-read based structural variant detection strategies 2022 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 4 citations Chemoenzymatic labeling of DNA methylation patterns for single-molecule epigenetic mapping 2022 Nucleic Acids Research article Biochemistry, Genetics and Molecular Biology Epigenetics and DNA Methylation Open access 33 citations Haplotype-resolved Chinese male genome assembly based on high-fidelity sequencing 2022 Fundamental Research article Biochemistry, Genetics and Molecular Biology Genomics and Phylogenetic Studies Open access 20 citations SVision: A deep learning approach to resolve complex structural variants 2022 Research Square preprint Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 2 citations Mako: A Graph-Based Pattern Growth Approach to Detect Complex Structural Variants 2021 Genomics Proteomics & Bioinformatics article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 9 citations Mako: a graph-based pattern growth approach to detect complex structural variants 2021 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 1 citations Haplotype threading: accurate polyploid phasing from long reads 2020 Genome biology article Biochemistry, Genetics and Molecular Biology Genomics and Phylogenetic Studies Open access 96 citations Long-read sequencing to understand genome biology and cell function 2020 The International Journal of Biochemistry & Cell Biology article Biochemistry, Genetics and Molecular Biology Genomics and Phylogenetic Studies 35 citations Haplotype Threading: Accurate Polyploid Phasing from Long Reads 2020 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genomics and Phylogenetic Studies Open access 18 citations 12 results References 0