Jinchen Li

Orcid: 0000-0003-3335-9303

According to our database1, Jinchen Li authored at least 15 papers between 2015 and 2026.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

Legend:

Book  In proceedings  Article  PhD thesis  Dataset  Other 

Links

On csauthors.net:

Bibliography

2026
Enhancing interpretation of clinical disease-associated copy number variations from multiple sequencing strategies with CNVSeeker.
Bioinform., 2026

2025
Rumor spreading model based on emotional characteristics and influence.
Expert Syst. Appl., 2025

Improved NB Model Analysis of Earthquake Recurrence Interval Coefficient of Variation for Major Active Faults in the Hetao Graben and Northern Marginal Region.
Entropy, 2025

Real-Time Motion Artifact Removal in fNIRS with Denoising Autoencoder at the Edge.
Proceedings of the IEEE International Symposium on Circuits and Systems, 2025

LEGO-Motion: Learning-Enhanced Grids with Occupancy Instance Modeling for Class-Agnostic Motion Prediction.
Proceedings of the IEEE/RSJ International Conference on Intelligent Robots and Systems, 2025

PBD: A Manually Curated Full-Chain Benchmark Dataset for Evaluating LLMs on ACMG PS3/BS3 Functional Evidence Acquisition.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2025

HCSeer2: A Deep Learning-Based Multi-Scale Modeling Framework for Predicting Cold and Hot Spots of Variants in the Human Exome.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2025

2024
KGNet: A Legal Knowledge Enhancement and GlobalPointer Triple Extraction Network.
Proceedings of the IEEE International Conference on Systems, Man, and Cybernetics, 2024

2023
Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-coding Variants.
Genom. Proteom. Bioinform., June, 2023

2022
Explainable artificial intelligence based on feature optimization for age at onset prediction of spinocerebellar ataxia type 3.
Frontiers Neuroinformatics, 2022

2020
Gene4Denovo: an integrated database and analytic platform for <i>de novo</i> mutations in humans.
Nucleic Acids Res., 2020

2018
VarCards: an integrated genetic and clinical database for coding variants in the human genome.
Nucleic Acids Res., 2018

CirGRDB: a database for the genome-wide deciphering circadian genes and regulators.
Nucleic Acids Res., 2018

2015
EpilepsyGene: a genetic resource for genes and mutations related to epilepsy.
Nucleic Acids Res., 2015

Sensitivity based image filtering for multi-hashing in large scale image retrieval problems.
Int. J. Mach. Learn. Cybern., 2015


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