Publications in Yadong Liu Group
2025
- GFHunter enables accurate and efficient gene fusion detection in long-read cancer transcriptomes. bioRxiv 2025. 链接
2024
- cuteFC: regenotyping structural variants through an accurate and efficient force-calling method. Genome Biology 2025. 链接
- A comprehensive genetic variant reference for the Chinese population. Science Bulletin 2024. 链接
- Comprehensive evaluation of haplotype phasing tools with different strategies across diverse sequence technologies. BIBM 2024. 链接
- Comprehensive Benchmarking of Genotype Imputation Tools Using a Large-Scale Chinese Reference Panel. BIBM 2024. 链接
- TDLM: A Diffusion Language Model for TCR Sequence Exploration and Generation. BIBM 2024. 链接
- miniSNV: accurate and fast single nucleotide variant calling from nanopore sequencing data. Briefings in Bioinformatics 2024. 链接
- MEHunter: transformer-based mobile element variant detection from long reads. Bioinformatics 2024. 链接
- HapKled: a haplotype-aware structural variant calling approach for Oxford nanopore sequencing data. Front. Genet. 2024. 链接
2023
- Kled: an ultra-fast and sensitive structural variant detection tool for long-read sequencing data. Briefings in Bioinformatics 2024. 链接
- A telomere-to-telomere genome assembly of Zhonghuang 13, a widely-grown soybean variety from the original center of Glycine max. The Crop Journal 2024. 链接
- Comprehensive evaluation of RNA-seq alignment methods based on long-read sequencing data. BIBM 2023. 链接
2022
- StackCirRNAPred: computational classification of long circRNA from other lncRNA based on stacking strategy. BMC Bioinformatics 2022. 链接
- Comparison of the Nanopore and PacBio sequencing technologies for DNA 5-methylcytosine detection. BIBM 2022. 链接
2021
- Long-read sequencing settings for efficient structural variation detection based on comprehensive evaluation. BMC Bioinformatics 2021. 链接
- SKSV: ultrafast structural variation detection from circular consensus sequencing reads. Bioinformatics 2021. 链接
- Psi-Caller: A Lightweight Short Read-Based Variant Caller With High Speed and Accuracy. Front. Cell Dev. Biol 2021. 链接
2020
- abPOA: an SIMD-based C library for fast partial order alignment using adaptive band. Bioinformatics 2020. 链接
- Long-read-based human genomic structural variation detection with cuteSV. Genome Biology 2020. 链接
2019
- deSALT: fast and accurate long transcriptomic read alignment with de Bruijn graph-based index. Genome Biology 2019. 链接
2016
- A neurodynamic approach to convex optimization problems with general constraint. Neural Networks 2016. 链接