Jingyang Gao

Orcid: 0000-0003-1270-6257

According to our database1, Jingyang Gao authored at least 32 papers between 2015 and 2024.

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

Timeline

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Bibliography

2024
ViroISDC: a method for calling integration sites of hepatitis B virus based on feature encoding.
BMC Bioinform., December, 2024

Deletion variants calling in third-generation sequencing data based on a dual-attention mechanism.
Briefings Bioinform., 2024

GGN-GO: geometric graph networks for predicting protein function by multi-scale structure features.
Briefings Bioinform., 2024

2023
DeepHipp: accurate segmentation of hippocampus using 3D dense-block based on attention mechanism.
BMC Medical Imaging, December, 2023

Lossless segmentation of cardiac medical images by a resolution consistent network with nondamage data preprocessing.
Multim. Tools Appl., 2023

2022
Gene Variation Detection Approach Based on Multimodal Data Fusion.
Proceedings of the Computer Science and Education - 17th International Conference, 2022

GcnSV: A Method Based on Deep Learning of Calling Structural Variations from the Third-Generation Sequencing Data.
Proceedings of the Computer Science and Education - 17th International Conference, 2022

2021
Cnngeno: A high-precision deep learning based strategy for the calling of structural variation genotype.
Comput. Biol. Chem., 2021

An efficient scRNA-seq dropout imputation method using graph attention network.
BMC Bioinform., 2021

IMDSVs: An integrated method based on machine learning and deep learning of calling structural variations from long-read data.
Proceedings of the 16th International Conference on Computer Science & Education, 2021

2020
Amplification Method of Lung Nodule Data Based on DCGAN Generation Algorithm.
Proceedings of the Data Science, 2020

iSchood: a Tool Software for Identifying Suspicious Copied Homework Documents with Definitive Contents.
Proceedings of the 15th International Conference on Computer Science & Education, 2020

A novel synonymous processing method based on amino acid substitution matrics for the classification of G-protein-coupled receptors.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2020

scSNVIndel. accurate and efficient calling of SNVs and indels from single cell sequencing using integrated Bi-LSTM.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2020

2019
DeepSV: accurate calling of genomic deletions from high-throughput sequencing data using deep convolutional neural network.
BMC Bioinform., 2019

Integrated Detection of Copy Number Variation Based on the Assembly of NGS and 3GS Data.
Proceedings of the Bioinformatics and Biomedical Engineering, 2019

CnnSV-Typer: Calling of Structural Variation Genotype Based on CUDA Acceleration.
Proceedings of the 21st IEEE International Conference on High Performance Computing and Communications; 17th IEEE International Conference on Smart City; 5th IEEE International Conference on Data Science and Systems, 2019

2018
基于深度学习的胃癌病理图像分类方法 (Pathological Image Classification of Gastric Cancer Based on Depth Learning).
计算机科学, 2018

Deletion genotype calling on the basis of sequence visualisation and image classification.
Int. J. Data Min. Bioinform., 2018

An Integrated Method of Detecting Copy Number Variation Based on Sequence Assembly.
Proceedings of the Intelligent Computing Theories and Application, 2018

GPU Parallelism of Phylogenetic Likelihood Estimates for Protein Data.
Proceedings of the 20th IEEE International Conference on High Performance Computing and Communications; 16th IEEE International Conference on Smart City; 4th IEEE International Conference on Data Science and Systems, 2018

Classification of G-protein Coupled Receptors Based on Semi-navïe Bayesian Inference.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018

cnnCNV: A Sensitive and Efficient Method for Detecting Copy Number Variation based on Convolutional Neural Networks.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018

2017
基于特征挖掘的基因组缺失变异集成检测方法 (Integrated Feature Mining Based Approach for Calling Genomic Deletions).
计算机科学, 2017

Concod: an effective integration framework of consensus-based calling deletions from next-generation sequencing data.
Int. J. Data Min. Bioinform., 2017

An efficient CNN-based classification on G-protein Coupled Receptors using TF-IDF and N-gram.
Proceedings of the 2017 IEEE Symposium on Computers and Communications, 2017

2016
MrBayes tgMC<sup>3</sup>++: A High Performance and Resource-Efficient GPU-Oriented Phylogenetic Analysis Method.
IEEE ACM Trans. Comput. Biol. Bioinform., 2016

Phylogenetic Likelihood Estimation on GPUs Using Vertical Partitioning Scheme.
Proceedings of the 2016 IEEE Trustcom/BigDataSE/ISPA, 2016

MrBayes 3.2.6 on Tianhe-1A: A High Performance and Distributed Implementation of Phylogenetic Analysis.
Proceedings of the 22nd IEEE International Conference on Parallel and Distributed Systems, 2016

Concod: Accurate consensus-based approach of calling deletions from high-throughput sequencing data.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2016

A high-precision shallow Convolutional Neural Network based strategy for the detection of Genomic Deletions.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2016

2015
A new INDEL detection strategy based on feature extraction.
J. Comput. Methods Sci. Eng., 2015


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