Yanpeng Yang

Mr. Yanpeng Yang

orcid

Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2023 in Computational and Structural Biotechnology Journal
Verified
Journal Article
Open access
YYYanpeng Yang
Yanpeng Yang
JLJian Li
Jian Li
Quan ZouQuan Zou
Quan Zou
YRYaoping Ruan
Yaoping Ruan
HFHailin Feng
Hailin Feng
The CRISPR/Cas9 system has significantly advanced the field of gene editing, yet its clinical application is constrained by the considerable challenge of off-target effects. Although numerous deep learning models for off-target prediction have been proposed, most struggle to effectively extract the nuanced features of guide RNA (gRNA) and DNA sequence pairs and to mitigate information loss during data transmission within the model. To address these limitations, we introduce a novel Hybrid Neural Network (HNN) model that employs a parallelized network structure to fully extract pertinent features from different positions and types of bases in the sequence to minimize information loss. Notably, this study marks the first application of word embedding techniques to extract information from sequence pairs that contain insertions and deletions (Indels). Comprehensive evaluation across diverse datasets indicates that our proposed model outperforms existing state-of-the-art prediction methods in off-target prediction. The datasets and source codes supporting this study can be found at https://github.com/Yang-k955/CRISPR-HW.

28 March 2025 in Genes
Verified
Journal Article
Open access
PDF file
YZYanyi Zheng
Yanyi Zheng
Quan ZouQuan Zou
Quan Zou
JLJian Li
Jian Li
YYYanpeng Yang
Yanpeng Yang
Background: The CRISPR-Cas9 system has emerged as one of the most promising gene-editing technologies in biology. However, off-target effects remain a significant challenge. While recent advances in deep learning have led to the development of models for off-target prediction, these models often fail to fully leverage sequence pair information. Furthermore, as the models’ parameter sizes increase, so do their complexities, limiting their practical applicability. Methods: In this study, we introduce a novel multi-feature independent encoding method, which encodes the gRNA-DNA sequence pair into three distinct feature matrices to minimize information loss. Additionally, we propose a lightweight hybrid deep learning framework, CRISPR-MFH, that integrates multi-scale separable convolutions and hybrid attention mechanisms for efficient and accurate off-target prediction. Results: Extensive experiments across multiple benchmark datasets demonstrate that the proposed encoding method effectively captures critical features and that CRISPR-MFH outperforms or matches state-of-the-art models with significantly fewer parameters across multiple evaluation metrics. Conclusions: This study offers a novel perspective for advancing deep learning technology in the realm of CRISPR-Cas9 off-target detection.