Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Genomics and Phylogenetic Studies, Genomics and Rare Diseases, and Cancer Genomics and Diagnostics.
Large-scale proteome inference from unpaired single-cell transcriptomic and proteomic data by msInfer
Using multimodal cortical parcellations to identify novel regions of the human cerebral cortex associated with cognitive performance.
cuteHap: Haplotype-Aware Structural Variant Detection in Phased Long-Read Sequencing Data.
cuteSV-OL: a real-time structural variation detection framework for nanopore sequencing devices.
GFSeeker: a splicing-graph-based approach for accurate gene fusion detection from long-read RNA sequencing data.
A comprehensive DNA methylation atlas for the Chinese population through nanopore long-read sequencing of 106 individuals
Cost-effective hybrid long- and short-read sequencing enables accurate somatic structural variant detection
HitSV: Maximizing discovery of structural variants across sequencing technologies
cuteFC: regenotyping structural variants through an accurate and efficient force-calling method.
Chromosome-scale and haplotype-resolved genome assembly of <i>Populus trichocarpa</i>.
A Biomass Graphene Composite Fluorescent Coating for Encryption of Anti-Counterfeit Information
SVHunter: long-read-based structural variation detection through the transformer model.
SVPG: A pangenome-based structural variant detection approach and rapid augmentation of pangenome graphs with new samples
Integrated Aerobic Exercise and Multisensory Environment Training for Age-related Cognitive Decline via Hippocampal-prefrontal Neural Circuit Modulation
MetaboLM: a metabolomic language model for multi-disease early prediction and risk stratification.
GFHunter enables accurate and efficient gene fusion detection in long-read cancer transcriptomes
CKG-TPI: integrating collaborative knowledge graph with sequence interactions for TCR-peptide binding specificity.
A telomere-to-telomere genome assembly of Zhonghuang 13, a widely-grown soybean variety from the original center of Glycine max
Kled: an ultra-fast and sensitive structural variant detection tool for long-read sequencing data
Kled: an ultra-fast and sensitive structural variant detection tool for long-read sequencing data.
A comprehensive genetic variant reference for the Chinese population.
SVDF: enhancing structural variation detect from long-read sequencing via automatic filtering strategies
SVDF: enhancing structural variation detect from long-read sequencing via automatic filtering strategies.
Long-read sequencing unveils novel somatic variants and methylation patterns in the genetic information system of early lung cancer.
DIRMC: a database of immunotherapy-related molecular characteristics.
miniSNV: accurate and fast single nucleotide variant calling from nanopore sequencing data.
MEHunter: transformer-based mobile element variant detection from long reads.
HapKled: a haplotype-aware structural variant calling approach for Oxford nanopore sequencing data.
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
BIR: Biomedical Information Retrieval System for Cancer Treatment in Electronic Health Record Using Transformers.