RESEARCH OUTPUT

Publications 15

Research papers, methods, and resources.

† Equal contribution   ·   * Corresponding author

2026*
Briefings in BioinformaticsIF 7.3 · 2025JCR Q1 · 2025↗

CRESCENT: a deep learning framework with multi-scale attention for detecting recurrent copy number alterations

Xikang Feng†*, Zheng Xu†, Sisi Peng, Jieyi Zheng, Chuan Ma, Qiangguo Jin*, Lingxi Chen*

copy number alterationsrecurrent CNAfocal CNAcancer analysisdeep learning
Abs
Abstract Recurrent copy number alterations (CNAs) are fundamental drivers of tumorigenesis, yet identifying them reliably remains a challenge due to the extreme variability in their genomic scale and context. Current methods often struggle to balance sensitivity across focal, segmental, and arm-level events. Here, we present CRESCENT, a deep learning framework designed to detect recurrent CNAs by integrating multi-scale sampling with convolutional neural networks and self-attention mechanisms. By processing copy number profiles from 7689 cases across 20 The Cancer Genome Atlas (TCGA) cancer projects, CRESCENT learns to distinguish recurrent drivers from background noise through parallel feature fusion. In rigorous leave-one-project-out cross-validation, the model demonstrated robust generalization, achieving area under the curves of 0.894–0.967 for amplifications and 0.804–0.929 for deletions in representative cohorts (Bladder Urothelial Carcinoma, Sarcoma, Glioblastoma Multiforme, Uterine Corpus Endometrial Carcinoma). Finally, extending beyond the TCGA-specific cross-validation, we trained a unified pan-cancer model to assess CRESCENT’s generalizability on simulated datasets and independent, non-TCGA cancer cohorts (CGCI and TARGET). Benchmarking against standard tools, including GISTIC2 and RUBIC, reveals that CRESCENT offers superior detection balance, identifying the highest total number of significant events across focal and broad scales. Moreover, extensive focal gene expression validation and pathway annotation, coupled with survival analysis, highlight that CRESCENT identifies critical oncogenic drivers and prognostic markers that conventional statistical methods often overlook. In all, CRESCENT provides a highly sensitive, generalized approach for decoding tumor evolution.
Bib
@article{doi_101093bibbbag167,
  title = {{CRESCENT: a deep learning framework with multi-scale attention for detecting recurrent copy number alterations}},
  author = {Xikang Feng and Zheng Xu and Sisi Peng and Jieyi Zheng and Chuan Ma and Qiangguo Jin and Lingxi Chen},
  journal = {Briefings in Bioinformatics},
  year = {2026},
  volume = {27},
  number = {2},
  doi = {10.1093/bib/bbag167},
  url = {https://doi.org/10.1093/bib/bbag167}
}
Journal metrics

BIOCHEMICAL RESEARCH METHODS JCR Q1 JIF rank 4/85

MATHEMATICAL & COMPUTATIONAL BIOLOGY JCR Q1 JIF rank 6/67

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2026*
Nucleic Acids ResearchIF 15.0 · 2025JCR Q1 · 2025↗

CNAScope: pan-cancer copy number aberration database with functional annotation and interactive visualization

Xikang Feng†*, Jieyi Zheng†, Sisi Peng†, Anna Jiang†, Ka Ho Ng, Chengshang Lyu, Qiangguo Jin*, Lingxi Chen*

copy number alterationsdatabase
Abs
Abstract Copy number aberrations (CNAs) are critical drivers of genomic diversity in oncology, where recurrent CNAs frequently underlie tumorigenesis. However, existing public resources are limited in their somatic CNA specificity, breadth across multiple data modalities, and support for recurrent CNAs with online functional annotation and interactive visualization. Here, we present CNAScope (https://cna.fengslab.com/), a database that curates and functionally annotates over 3 954 361 CNA profiles and 3 946 319 metadata from 810 datasets, 174 464 samples, 3 018 672 single cells, and 764 232 spatial cells/spots, spanning 77 cancer subtypes from eight data sources and 55 cancer initiatives and institutions. CNAScope offers downloadable CNA annotations and interactive visualizations at bin, gene, and pathway term levels, including phylogenetic inference, clustering, dimension reduction, and focal/consensus CNA detection. Users can explore data through interactive heatmaps, phylogenetic trees, embedding plots, CN charts, and focal/consensus plots, or upload and annotate their own CNAs in real time. In all, with its large curated data volume and rich annotation capabilities, CNAScope serves as a vital resource for accelerating cancer research.
Bib
@article{doi_101093nargkaf1242,
  title = {{CNAScope: pan-cancer copy number aberration database with functional annotation and interactive visualization}},
  author = {Xikang Feng and Jieyi Zheng and Sisi Peng and Anna Jiang and Ka Ho Ng and Chengshang Lyu and Qiangguo Jin and Lingxi Chen},
  journal = {Nucleic Acids Research},
  year = {2026},
  volume = {54},
  number = {D1},
  pages = {D1364-D1375},
  doi = {10.1093/nar/gkaf1242},
  url = {https://doi.org/10.1093/nar/gkaf1242}
}
Journal metrics

BIOCHEMISTRY & MOLECULAR BIOLOGY JCR Q1 JIF rank 14/328

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2026*
Nucleic Acids ResearchIF 15.0 · 2025JCR Q1 · 2025↗

MicrobialScope: an integrated genomic resource with rich annotations across bacteria, archaea, fungi, and viruses

Xikang Feng†, Yinhu Li†, Jieyi Zheng†, Xuhua Chen†, Shuo Yang, Yu Chen*, Shuai Cheng Li*

Abs
Abstract Microorganisms, including bacteria, archaea, fungi, and viruses, are the most taxonomically diverse and ecologically dominant life forms on Earth, playing critical roles in ecosystems, human health, and industrial applications. While existing microbial databases such as BV-BRC and IMG archive both monoisolate and metagenome-assembled genomes (MAGs) across domains, challenges remain in standardized, multi-level annotations and interactive tools for all microbial groups. Here, we present MicrobialScope (https://microbial.deepomics.org/), a comprehensive microbial genomic platform that integrates large-scale genome collections, multilevel annotations, and interactive visualizations. MicrobialScope harbors 2 411 503 bacterial, 24 472 archaeal, 20 203 fungal, and 188 267 viral genomes derived from both monoisolate assemblies and MAGs. Integrating 15 state-of-the-art bioinformatics tools and 10 specialized databases, MicrobialScope provides extensive annotations encompassing basic genomic features, genomic element prediction (e.g., genes, tRNAs, tmRNAs, CRISPR–Cas and anti-CRISPR elements, secondary metabolite biosynthetic clusters, signal peptides, and transmembrane proteins), and functional and structural annotations. This includes 1 072 114 935 proteins with diverse annotations, 24 640 186 tRNAs and tmRNAs, 140 888 CRISPR–Cas systems, 173 256 anti-CRISPR elements, 105 121 secondary metabolite biosynthetic clusters, 13 235 096 signal peptides, and 50 811 729 transmembrane proteins. In addition, MicrobialScope offers unrestricted access to all data resources, interactive visualization tools, and built-in online analytical modules for intuitive exploration and comparative analysis. With its extensive genome collection, comprehensive annotations, and user-friendly interface, MicrobialScope serves as a scalable platform to advance genome research across diverse microbial domains.
Bib
@article{doi_101093nargkaf1234,
  title = {{MicrobialScope: an integrated genomic resource with rich annotations across bacteria, archaea, fungi, and viruses}},
  author = {Xikang Feng and Yinhu Li and Jieyi Zheng and Xuhua Chen and Shuo Yang and Yu Chen and Shuai Cheng Li},
  journal = {Nucleic Acids Research},
  year = {2026},
  volume = {54},
  number = {D1},
  pages = {D842-D851},
  doi = {10.1093/nar/gkaf1234},
  url = {https://doi.org/10.1093/nar/gkaf1234}
}
Journal metrics

BIOCHEMISTRY & MOLECULAR BIOLOGY JCR Q1 JIF rank 14/328

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2024*
Briefings in BioinformaticsIF 7.3 · 2025JCR Q1 · 2025↗

A comprehensive benchmarking for evaluating TCR embeddings in modeling TCR-epitope interactions

Xikang Feng†*, Miaozhe Huo†, He Li, Yongze Yang, Yuepeng Jiang, Liang He, Shuai Cheng Li*

Abs
Abstract The complexity of T cell receptor (TCR) sequences, particularly within the complementarity-determining region 3 (CDR3), requires efficient embedding methods for applying machine learning to immunology. While various TCR CDR3 embedding strategies have been proposed, the absence of their systematic evaluations created perplexity in the community. Here, we extracted CDR3 embedding models from 19 existing methods and benchmarked these models with four curated datasets by accessing their impact on the performance of TCR downstream tasks, including TCR-epitope binding affinity prediction, epitope-specific TCR identification, TCR clustering, and visualization analysis. We assessed these models utilizing eight downstream classifiers and five downstream clustering methods, with the performance measured by a diverse range of metrics for precision, robustness, and usability. Overall, handcrafted embeddings outperformed data-driven ones in modeling TCR-epitope interactions. To further refine our comparative findings, we developed an all-in-one TCR CDR3 embedding package comprising all evaluated embedding models. This package will assist users in easily selecting suitable embedding models for their data.
Bib
@article{doi_101093bibbbaf030,
  title = {{A comprehensive benchmarking for evaluating TCR embeddings in modeling TCR-epitope interactions}},
  author = {Xikang Feng and Miaozhe Huo and He Li and Yongze Yang and Yuepeng Jiang and Liang He and Shuai Cheng Li},
  journal = {Briefings in Bioinformatics},
  year = {2024},
  volume = {26},
  number = {1},
  doi = {10.1093/bib/bbaf030},
  url = {https://doi.org/10.1093/bib/bbaf030}
}
Journal metrics

BIOCHEMICAL RESEARCH METHODS JCR Q1 JIF rank 4/85

MATHEMATICAL & COMPUTATIONAL BIOLOGY JCR Q1 JIF rank 6/67

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2024
Nucleic Acids ResearchIF 15.0 · 2025JCR Q1 · 2025↗

PlasmidScope: a comprehensive plasmid database with rich annotations and online analytical tools

Yinhu Li†, Xikang Feng†, Xuhua Chen†, Shuo Yang, Zicheng Zhao, Yu Chen*, Shuai Cheng Li*

Bib
@article{feng2024_5,
  title = {{PlasmidScope: a comprehensive plasmid database with rich annotations and online analytical tools}},
  author = {Yinhu Li and Xikang Feng and Xuhua Chen and Shuo Yang and Zicheng Zhao and Yu Chen and Shuai Cheng Li},
  journal = {Nucleic Acids Research},
  year = {2024},
  doi = {10.1093/nar/gkae930},
  url = {https://doi.org/10.1093/nar/gkae930}
}
Journal metrics

BIOCHEMISTRY & MOLECULAR BIOLOGY JCR Q1 JIF rank 14/328

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2023
Journal of Integrative AgricultureIF 5.7 · 2025JCR Q1 · 2025↗

SCSMRD: A database for single-cell skeletal muscle regeneration

Xikang Feng, Chundi Xie, Yongyao Li, Zishuai Wang*, Lijing Bai*

Bib
@article{feng2023_6,
  title = {{SCSMRD: A database for single-cell skeletal muscle regeneration}},
  author = {Xikang Feng and Chundi Xie and Yongyao Li and Zishuai Wang and Lijing Bai},
  journal = {Journal of Integrative Agriculture},
  year = {2023},
  url = {https://www.sciencedirect.com/science/article/pii/S2095311922001861}
}
Journal metrics

AGRICULTURE, MULTIDISCIPLINARY JCR Q1 JIF rank 18/95

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2022
BMC GenomicsIF 3.9 · 2025JCR Q2 · 2025↗

SCSilicon: a tool for synthetic single-cell DNA sequencing data generation

Xikang Feng†*, Lingxi Chen†

Bib
@article{feng2022_7,
  title = {{SCSilicon: a tool for synthetic single-cell DNA sequencing data generation}},
  author = {Xikang Feng and Lingxi Chen},
  journal = {BMC Genomics},
  year = {2022},
  doi = {10.1186/s12864-022-08566-w},
  url = {https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08566-w}
}
Journal metrics

BIOTECHNOLOGY & APPLIED MICROBIOLOGY JCR Q2 JIF rank 75/180

GENETICS & HEREDITY JCR Q2 JIF rank 57/192

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2021
Journal of intensive careIF 7.5 · 2025JCR Q1 · 2025↗

Development and validation of an online model to predict critical COVID-19 with immune-inflammatory parameters

Yue Gao†, Lingxi Chen†, Jianhua Chi†, Shaoqing Zeng†, Xikang Feng, Huayi Li, Dan Liu, Xinxia Feng, Siyuan Wang, Ya Wang, Ruidi Yu, Yuan Yuan, Sen Xu, Chunrui Li, Wei Zhang*, Shuaicheng Li*, Qinglei Gao*

Bib
@article{feng2021_8,
  title = {{Development and validation of an online model to predict critical COVID-19 with immune-inflammatory parameters}},
  author = {Yue Gao and Lingxi Chen and Jianhua Chi and Shaoqing Zeng and Xikang Feng and Huayi Li and Dan Liu and Xinxia Feng and Siyuan Wang and Ya Wang and Ruidi Yu and Yuan Yuan and Sen Xu and Chunrui Li and Wei Zhang and Shuaicheng Li and Qinglei Gao},
  journal = {Journal of intensive care},
  year = {2021},
  doi = {10.1186/s40560-021-00531-1},
  url = {https://jintensivecare.biomedcentral.com/articles/10.1186/s40560-021-00531-1}
}
Journal metrics

CRITICAL CARE MEDICINE JCR Q1 JIF rank 8/66

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2021
Briefings in BioinformaticsIF 7.3 · 2025JCR Q1 · 2025↗

Deep learning model reveals potential risk genes for ADHD, especially Ephrin receptor gene EPHA5

Lu Liu†, Xikang Feng†, Haimei Li, Shuai Cheng Li*, Qiujin Qian*, Yufeng Wang*

Bib
@article{feng2021_9,
  title = {{Deep learning model reveals potential risk genes for ADHD, especially Ephrin receptor gene EPHA5}},
  author = {Lu Liu and Xikang Feng and Haimei Li and Shuai Cheng Li and Qiujin Qian and Yufeng Wang},
  journal = {Briefings in Bioinformatics},
  year = {2021},
  doi = {10.1093/bib/bbab207},
  url = {https://academic.oup.com/bib/article-abstract/22/6/bbab207/6295376}
}
Journal metrics

BIOCHEMICAL RESEARCH METHODS JCR Q1 JIF rank 4/85

MATHEMATICAL & COMPUTATIONAL BIOLOGY JCR Q1 JIF rank 6/67

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2021
BMC GenomicsIF 3.9 · 2025JCR Q2 · 2025↗

SCYN: single cell cnv profiling method using dynamic programming

Xikang Feng†, Lingxi Chen†, Yuhao Qing, Ruikang Li, Chaohui Li, Shuai Cheng Li*

Bib
@article{feng2021_10,
  title = {{SCYN: single cell cnv profiling method using dynamic programming}},
  author = {Xikang Feng and Lingxi Chen and Yuhao Qing and Ruikang Li and Chaohui Li and Shuai Cheng Li},
  journal = {BMC Genomics},
  year = {2021},
  doi = {10.1186/s12864-021-07941-3},
  url = {https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-021-07941-3}
}
Journal metrics

BIOTECHNOLOGY & APPLIED MICROBIOLOGY JCR Q2 JIF rank 75/180

GENETICS & HEREDITY JCR Q2 JIF rank 57/192

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2020
BMC GenomicsIF 3.9 · 2025JCR Q2 · 2025↗

I-Impute: a self-consistent method to impute single cell RNA sequencing data

Xikang Feng†, Lingxi Chen†, Zishuai Wang, Shuai Cheng Li*

Bib
@article{feng2020_11,
  title = {{I-Impute: a self-consistent method to impute single cell RNA sequencing data}},
  author = {Xikang Feng and Lingxi Chen and Zishuai Wang and Shuai Cheng Li},
  journal = {BMC Genomics},
  year = {2020},
  doi = {10.1186/s12864-020-07007-w},
  url = {https://link.springer.com/article/10.1186/s12864-020-07007-w}
}
Journal metrics

BIOTECHNOLOGY & APPLIED MICROBIOLOGY JCR Q2 JIF rank 75/180

GENETICS & HEREDITY JCR Q2 JIF rank 57/192

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

2020
Clinical and translational medicineIF 7.9 · 2025JCR Q1 · 2025↗

CIRPMC: an online model with simplified inflammatory signature to predict the occurrence of critical illness in patients with COVID‐19

Yue Gao†, Lingxi Chen†, Shaoqing Zeng†, Xikang Feng†, JianHua Chi†, Ya Wang, Huayi Li, Tengping Jiang, Yang Yu, XiaoFei Jiao, Dan Liu, XinXia Feng, SiYuan Wang, RuiDi Yu, Yuan Yuan, Sen Xu, Guangyao Cai, Xiaoming Xiong, Pingbo Chen, Qingqing Mo, Xin Jin, Yuan Wu, Ding Ma, Chunrui Li, Shuai Cheng Li*, Qinglei Gao*

Bib
@article{feng2020_12,
  title = {{CIRPMC: an online model with simplified inflammatory signature to predict the occurrence of critical illness in patients with COVID‐19}},
  author = {Yue Gao and Lingxi Chen and Shaoqing Zeng and Xikang Feng and JianHua Chi and Ya Wang and Huayi Li and Tengping Jiang and Yang Yu and XiaoFei Jiao and Dan Liu and XinXia Feng and SiYuan Wang and RuiDi Yu and Yuan Yuan and Sen Xu and Guangyao Cai and Xiaoming Xiong and Pingbo Chen and Qingqing Mo and Xin Jin and Yuan Wu and Ding Ma and Chunrui Li and Shuai Cheng Li and Qinglei Gao},
  journal = {Clinical and translational medicine},
  year = {2020},
  doi = {10.1002/ctm2.210},
  url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/ctm2.210}
}
Journal metrics

MEDICINE, RESEARCH & EXPERIMENTAL JCR Q1 JIF rank 25/191

ONCOLOGY JCR Q1 JIF rank 45/333

2025 annual data · ShowJCR community dataset · Retrieved 2026-10-09 · Source ↗

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