Ethan Jacob Moyer
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Ethan Jacob Moyer has a total of 48 co-authors. Here are the top co-authors by number of shared publications:
- Daniel Schwartz
Drexel University
4 shared publications Adam Dunlop
College of Arts & Sciences, Drexel University, PA
2 shared publications- Alex Zavalny
College of Computing and Informatics, Drexel University
2 shared publications - Alisha Isabelle Augustin
College of Engineering, Drexel University
2 shared publications - Brandon Gorski
College of Computing and Informatics, Drexel University
2 shared publications - Edward Kim
College of Computing and Informatics, Drexel University
2 shared publications
Latest Publications
- Open Access
- 24 October 2025
- Published by American Association for the Advancement of Science (AAAS) in Science Advances
- Vol. 11 (43) , eadw3027
KnowYourCG: Facilitating base-level sparse methylome interpretation
Decoding DNA methylomes for biological insights is critical in epigenetics research. We present KnowYourCG (KYCG), a data interpretation framework designed for functional DNA methylation analysis. Unlike existing tools that target genes or genomic intervals, KYCG features direct base-level screenings of diverse biological and technical influences, including sequence motifs, transcription factor binding, histone modifications, replication timing, cell-type–specific methylation, and trait associations. Through implementing efficient infrastructure that rapidly screens and investigates thousands of knowledgebases, KYCG addresses the challenges of data sparsity in various methylation datasets, including low-pass or single-cell DNA methylomes, 5-hydroxymethylation (5hmC) profiles, spatial DNA methylation maps, and array-based datasets for epigenome-wide association studies. Applying KYCG to these datasets provides valuable insights into cell differentiation, cancer origins, epigenome-trait associations, and technical issues such as array artifacts, single-cell batch effects, and Nanopore 5hmC detection accuracy. Our tool simplifies large-scale methylation analysis and integrates seamlessly with standard assay technologies.
- 24 October 2025
- Published by American Association for the Advancement of Science (AAAS) in Science Advances
- Vol. 11 (43) , eadw3027
Open AccessKnowYourCG: Facilitating base-level sparse methylome interpretation
Decoding DNA methylomes for biological insights is critical in epigenetics research. We present KnowYourCG (KYCG), a data interpretation framework designed for functional DNA methylation analysis. Unlike existing tools that target genes or genomic intervals, KYCG features direct base-level screenings of diverse biological and technical influences, including sequence motifs, transcription factor binding, histone modifications, replication timing, cell-type–specific methylation, and trait associations. Through implementing efficient infrastructure that rapidly screens and investigates thousands of knowledgebases, KYCG addresses the challenges of data sparsity in various methylation datasets, including low-pass or single-cell DNA methylomes, 5-hydroxymethylation (5hmC) profiles, spatial DNA methylation maps, and array-based datasets for epigenome-wide association studies. Applying KYCG to these datasets provides valuable insights into cell differentiation, cancer origins, epigenome-trait associations, and technical issues such as array artifacts, single-cell batch effects, and Nanopore 5hmC detection accuracy. Our tool simplifies large-scale methylation analysis and integrates seamlessly with standard assay technologies.
- Open Access
- 31 August 2022
- Published by Elsevier in Informatics in Medicine Unlocked
- Vol. 33
RadGenNets: Deep learning-based radiogenomics model for gene mutation prediction in lung cancer
- 31 August 2022
- Published by Elsevier in Informatics in Medicine Unlocked
- Vol. 33
Open AccessRadGenNets: Deep learning-based radiogenomics model for gene mutation prediction in lung cancer
- Open Access
- 13 July 2022
- Published by Elsevier in Cell Genomics
- Vol. 2 (7)
DNA methylation dynamics and dysregulation delineated by high-throughput profiling in the mouse
- 13 July 2022
- Published by Elsevier in Cell Genomics
- Vol. 2 (7)
Open AccessDNA methylation dynamics and dysregulation delineated by high-throughput profiling in the mouse
- Open Access
RadGenNets: Deep Learning-Based Radiogenomics Model For Gene Mutation Prediction In Lung Cancer
A bstract: In this paper, we present our methodology that can be used for predicting gene mutation in patients with non-small cell lung cancer (NSCLC). There are three major types of gene mutations that a NSCLC patient’s gene structure can change to: epidermal growth factor receptor (EGFR), Kirsten rat sarcoma virus (KRAS), and Anaplastic lymphoma kinase (ALK). We worked with the clinical and genomics data for each patient as well CT scans. We preprocessed all of the data and then built a novel pipeline to integrate both the image and tabular data. We built a novel pipeline that used a fusion of Convolutional Neural Networks and Dense Neural Networks. Also, using a search approach, we pick an ensemble of deep learning models to classify the separate gene mutations. These models include EfficientNets, SENet, and ResNeXt WSL, among others. Our model achieved a high area under curve (AUC) score of 94% in detecting gene mutation.
Open AccessRadGenNets: Deep Learning-Based Radiogenomics Model For Gene Mutation Prediction In Lung Cancer
A bstract: In this paper, we present our methodology that can be used for predicting gene mutation in patients with non-small cell lung cancer (NSCLC). There are three major types of gene mutations that a NSCLC patient’s gene structure can change to: epidermal growth factor receptor (EGFR), Kirsten rat sarcoma virus (KRAS), and Anaplastic lymphoma kinase (ALK). We worked with the clinical and genomics data for each patient as well CT scans. We preprocessed all of the data and then built a novel pipeline to integrate both the image and tabular data. We built a novel pipeline that used a fusion of Convolutional Neural Networks and Dense Neural Networks. Also, using a search approach, we pick an ensemble of deep learning models to classify the separate gene mutations. These models include EfficientNets, SENet, and ResNeXt WSL, among others. Our model achieved a high area under curve (AUC) score of 94% in detecting gene mutation.
- Open Access
- 18 July 2021
- Published by Institute of Electrical and Electronics Engineers (IEEE)
- p. 1-8
Towards Searching Efficient and Accurate Neural Network Architectures in Binary Classification Problems
In recent years, deep neural networks have had great success in machine learning and pattern recognition. Architecture size for a neural network contributes significantly to the success of neural networks. In this study, we optimize the selection process by investigating different search algorithms to find a neural network architecture size that yields the highest accuracy. We apply binary search on a very well-defined binary classification network search space and compare the results to those of linear search. We also propose how to relax some of the assumptions regarding the data set so that our solution can be generalized to any binary classification problem. We report a 100-fold running time improvement over the naive linear search when we apply the binary search method to our data sets in order to find the best architecture candidate. By finding the optimal architecture for any binary classification problem quickly, we hope that our research contributes to discovering intelligent algorithms for optimizing architecture selection in machine learning.
- 18 July 2021
- Published by Institute of Electrical and Electronics Engineers (IEEE)
- p. 1-8
Open AccessTowards Searching Efficient and Accurate Neural Network Architectures in Binary Classification Problems
In recent years, deep neural networks have had great success in machine learning and pattern recognition. Architecture size for a neural network contributes significantly to the success of neural networks. In this study, we optimize the selection process by investigating different search algorithms to find a neural network architecture size that yields the highest accuracy. We apply binary search on a very well-defined binary classification network search space and compare the results to those of linear search. We also propose how to relax some of the assumptions regarding the data set so that our solution can be generalized to any binary classification problem. We report a 100-fold running time improvement over the naive linear search when we apply the binary search method to our data sets in order to find the best architecture candidate. By finding the optimal architecture for any binary classification problem quickly, we hope that our research contributes to discovering intelligent algorithms for optimizing architecture selection in machine learning.
- Open Access
Towards Searching Efficient and Accurate Neural Network Architectures in Binary Classification Problems
In recent years, deep neural networks have had great success in machine learning and pattern recognition. Architecture size for a neural network contributes significantly to the success of any neural network. In this study, we optimize the selection process by investigating different search algorithms to find a neural network architecture size that yields the highest accuracy. We apply binary search on a very well-defined binary classification network search space and compare the results to those of linear search. We also propose how to relax some of the assumptions regarding the dataset so that our solution can be generalized to any binary classification problem. We report a 100-fold running time improvement over the naive linear search when we apply the binary search method to our datasets in order to find the best architecture candidate. By finding the optimal architecture size for any binary classification problem quickly, we hope that our research contributes to discovering intelligent algorithms for optimizing architecture size selection in machine learning.
Open AccessTowards Searching Efficient and Accurate Neural Network Architectures in Binary Classification Problems
In recent years, deep neural networks have had great success in machine learning and pattern recognition. Architecture size for a neural network contributes significantly to the success of any neural network. In this study, we optimize the selection process by investigating different search algorithms to find a neural network architecture size that yields the highest accuracy. We apply binary search on a very well-defined binary classification network search space and compare the results to those of linear search. We also propose how to relax some of the assumptions regarding the dataset so that our solution can be generalized to any binary classification problem. We report a 100-fold running time improvement over the naive linear search when we apply the binary search method to our datasets in order to find the best architecture candidate. By finding the optimal architecture size for any binary classification problem quickly, we hope that our research contributes to discovering intelligent algorithms for optimizing architecture size selection in machine learning.