Qinghua Jiang
Orcid: 0000-0002-1827-0389
According to our database1,
Qinghua Jiang
authored at least 44 papers
between 2009 and 2023.
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Bibliography
2023
DeepCCI: a deep learning framework for identifying cell-cell interactions from single-cell RNA sequencing data.
Bioinform., October, 2023
An interpretable single-cell RNA sequencing data clustering method based on latent Dirichlet allocation.
Briefings Bioinform., July, 2023
Single-cell transcriptomics reveals the interaction between peripheral CD4<sup>+</sup> CTLs and mesencephalic endothelial cells mediated by IFNG in Parkinson's disease.
Comput. Biol. Medicine, May, 2023
Integrated smart analytics of nucleic acid amplification tests <i>via</i> paper microfluidics and deep learning in cloud computing.
Biomed. Signal Process. Control., May, 2023
An Integrated Calibration Scheme for Attitude Benchmark of Micro-nano Satellites and Its Experiments Based on In-Orbit Data.
Proceedings of the 8th International Conference on Automation, 2023
2022
An efficient multilayer RBF neural network and its application to regression problems.
Neural Comput. Appl., 2022
MutCov: A pipeline for evaluating the effect of mutations in spike protein on infectivity and antigenicity of SARS-CoV-2.
Comput. Biol. Medicine, 2022
Network analysis between neuron dysfunction and neuroimmune response based on neural single-cell transcriptome of COVID-19 patients.
Comput. Biol. Medicine, 2022
Overview of structural variation calling: Simulation, identification, and visualization.
Comput. Biol. Medicine, 2022
Briefings Bioinform., 2022
CBLRR: a cauchy-based bounded constraint low-rank representation method to cluster single-cell RNA-seq data.
Briefings Bioinform., 2022
Identification of alternative splicing-derived cancer neoantigens for mRNA vaccine development.
Briefings Bioinform., 2022
2021
Identification of sub-Golgi protein localization by use of deep representation learning features.
Bioinform., 2021
DLpTCR: an ensemble deep learning framework for predicting immunogenic peptide recognized by T cell receptor.
Briefings Bioinform., 2021
Global characterization of B cell receptor repertoire in COVID-19 patients by single-cell V(D)J sequencing.
Briefings Bioinform., 2021
Comprehensive analysis of partial methylation domains in colorectal cancer based on single-cell methylation profiles.
Briefings Bioinform., 2021
Proceedings of the IEEE International Conference on Signal Processing, 2021
2020
ERDS-Exome: A Hybrid Approach for Copy Number Variant Detection from Whole-Exome Sequencing Data.
IEEE ACM Trans. Comput. Biol. Bioinform., 2020
Morbigenous brain region and gene detection with a genetically evolved random neural network cluster approach in late mild cognitive impairment.
Bioinform., 2020
2019
LncRNA2Target v2.0: a comprehensive database for target genes of lncRNAs in human and mouse.
Nucleic Acids Res., 2019
ProbPFP: a multiple sequence alignment algorithm combining hidden Markov model optimized by particle swarm optimization with partition function.
BMC Bioinform., 2019
BIN1 rs744373 variant shows different association with Alzheimer's disease in Caucasian and Asian populations.
BMC Bioinform., 2019
A learning-based framework for miRNA-disease association identification using neural networks.
Bioinform., 2019
2018
Disease status affects the association between rs4813620 and the expression of Alzheimer's disease susceptibility gene <i>TRIB3</i>.
Proc. Natl. Acad. Sci. USA, 2018
DincRNA: a comprehensive web-based bioinformatics toolkit for exploring disease associations and ncRNA function.
Bioinform., 2018
CircR2Disease: a manually curated database for experimentally supported circular RNAs associated with various diseases.
Database J. Biol. Databases Curation, 2018
BIN1 rs744373 Variant Is Significantly Associated with Alzheimer's Disease in Caucasian but Not East Asian Populations.
Proceedings of the Intelligent Computing Theories and Application, 2018
ProbPFP: A Multiple Sequence Alignment Algorithm Combining Partition Function and Hidden Markov Model with Particle Swarm Optimization.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018
2017
DTWscore: differential expression and cell clustering analysis for time-series single-cell RNA-seq data.
BMC Bioinform., 2017
GED: a manually curated comprehensive resource for epigenetic modification of gametogenesis.
Briefings Bioinform., 2017
2016
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2016
ERDS-pe: A paired hidden Markov model for copy number variant detection from whole-exome sequencing data.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2016
InfDisSim: A novel method for measuring disease similarity based on information flow.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2016
2015
LncRNA2Target: a database for differentially expressed genes after lncRNA knockdown or overexpression.
Nucleic Acids Res., 2015
misFinder: identify mis-assemblies in an unbiased manner using reference and paired-end reads.
BMC Bioinform., 2015
2014
BMC Syst. Biol., 2014
Proceedings of the 2nd International Conference on Systems and Informatics, 2014
2013
Int. J. Data Min. Bioinform., 2013
2010
Sensors, 2010
BMC Syst. Biol., 2010
Proceedings of the Fifth International Conference on Frontier of Computer Science and Technology, 2010
Proceedings of the 2010 IEEE International Conference on Bioinformatics and Biomedicine, 2010
2009
Nucleic Acids Res., 2009