Tao Jiang
Orcid: 0000-0002-0673-8503Affiliations:
- Harbin Institute of Technology, School of Computer Science and Technology, China (PhD 2019)
According to our database1,
Tao Jiang authored at least 27 papers
between 2017 and 2026.
Collaborative distances:
Collaborative distances:
Timeline
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Book In proceedings Article PhD thesis Dataset OtherLinks
Online presence:
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on orcid.org
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on github.com
On csauthors.net:
Bibliography
2026
cuteSV-OL: a real-time structural variation detection framework for nanopore sequencing devices.
Bioinform., 2026
GFSeeker: a splicing-graph-based approach for accurate gene fusion detection from long-read RNA sequencing data.
Briefings Bioinform., 2026
2025
SVHunter: long-read-based structural variation detection through the transformer model.
Briefings Bioinform., May, 2025
CKG-TPI: integrating collaborative knowledge graph with sequence interactions for TCR-peptide binding specificity.
Briefings Bioinform., 2025
DNAMatch: An Ultra-Fast and Memory-Efficient Deep Learning Framework for Aligning Ultra-Long DNA Fragments.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2025
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2025
MethSV: A Long-Read-Based Framework for Profiling DNA Methylation in Structural Variation.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2025
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2025
2024
miniSNV: accurate and fast single nucleotide variant calling from nanopore sequencing data.
Briefings Bioinform., November, 2024
SVDF: enhancing structural variation detect from long-read sequencing via automatic filtering strategies.
Briefings Bioinform., July, 2024
Kled: an ultra-fast and sensitive structural variant detection tool for long-read sequencing data.
Briefings Bioinform., March, 2024
Database J. Biol. Databases Curation, January, 2024
Bioinform., 2024
Comprehensive evaluation of haplotype phasing tools with different strategies across diverse sequence technologies.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2024
Comprehensive Benchmarking of Genotype Imputation Tools Using a Large-Scale Chinese Reference Panel.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2024
2023
BIR: Biomedical Information Retrieval System for Cancer Treatment in Electronic Health Record Using Transformers.
Sensors, December, 2023
Reply: Correspondence on NanoVar's performance outlined by Jiang T. et al. in 'Long-read sequencing settings for efficient structural variation detection based on comprehensive evaluation'.
BMC Bioinform., December, 2023
Identifying cancer driver genes using a two-stage random walk with restart on a gene interaction network.
Comput. Biol. Medicine, May, 2023
Comprehensive evaluation of RNA-seq alignment methods based on long-read sequencing data.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2023
2022
Evaluation of classification in single cell atac-seq data with machine learning methods.
BMC Bioinform., 2022
Comparison of the Nanopore and PacBio sequencing technologies for DNA 5-methylcytosine detection.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2022
2021
Long-read sequencing settings for efficient structural variation detection based on comprehensive evaluation.
BMC Bioinform., 2021
SKSV: ultrafast structural variation detection from circular consensus sequencing reads.
Bioinform., 2021
2020
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2020
2019
Bioinform., 2019
2018
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018
2017
rMFilter: acceleration of long read-based structure variation calling by chimeric read filtering.
Bioinform., 2017