日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Harnessing artificial intelligence for genomic variant prediction: advances, challenges, and future directions

利用人工智能进行基因组变异预测:进展、挑战和未来方向

Pakpahan, Indah; Sihombing, Mentari; Liu, Haohan; Wang, Mengyao; Su, Zheng; Fang, Mingyan

The development of a situation-specific theory of dynamic interactions for multimorbid dyads in Chinese family culture

针对中国家庭文化中多重疾病二元关系的动态互动情境特定理论的发展

Fang, Mingyan; Jin, Yuanyuan; Liu, Zhiyu; Song, Junyang; Li, Huiling

Genetic and clinical determinants of neonatal jaundice and growth patterns in the Qingdao birth cohort: A genome-wide association study

青岛出生队列中新生儿黄疸和生长模式的遗传和临床决定因素:一项全基因组关联研究

Chen, Xu; Du, Peina; Li, Shuo; Wang, Xiaohong; Xu, Mengyang; Chu, Zhaobin; Zhang, Yue; Yao, Zhengyang; Huan, Xuejie; Huang, Yushan; Fang, Mingyan; Gao, Ya; Fan, Guangyi; Jin, Xin; Huang, Hui; Pan, Silin

GeneRAIN: multifaceted representation of genes via deep learning of gene expression networks

GeneRAIN:通过基因表达网络的深度学习实现基因的多方面表征

Su, Zheng; Fang, Mingyan; Smolnikov, Andrei; Dinger, Marcel E; Oates, Emily C; Vafaee, Fatemeh

Whole-genome Sequencing Association Analysis of Quantitative Platelet Traits in A Large Cohort of β-thalassemia

对大型β-地中海贫血队列中血小板定量性状进行全基因组测序关联分析

Wang, Xingmin; Zhang, Qianqian; Chen, Xianming; Huang, Yushan; Zhang, Wei; Liao, Liuhua; Zhang, Xinhua; Huang, Binbin; Huang, Yueyan; Ye, Yuhua; Song, Mengyang; Lao, Jinquan; Chen, Juanjuan; Feng, Xiaoqin; Long, Xingjiang; Liu, Zhixiang; Zhu, Weijian; Yu, Lian; Fan, Chengwu; Tang, Deguo; Zhong, Tianyu; Fang, Mingyan; Li, Caiyun; Niu, Chao; Huang, Li; Lin, Bin; Hua, Xiaoyun; Jin, Xin; Li, Zilin; Xu, Xiangmin

Age-Related Dynamics and Spectral Characteristics of the TCRβ Repertoire in Healthy Children: Implications for Immune Aging

健康儿童TCRβ库的年龄相关动态和光谱特征:对免疫衰老的启示

Fang, Mingyan; Miao, Yu; Zhu, Lin; Mei, Yunpeng; Zeng, Hui; Luo, Lihua; Ding, Yuan; Zhou, Lina; Quan, Xueping; Zhao, Qin; Zhao, Xiaodong; An, Yunfei

Shared genetic features inference among hypoxia-ischemia diseases in the presence of heterogenous omics data based on a novel risk assessment method

基于一种新型风险评估方法,在存在异质组学数据的情况下推断缺氧缺血性疾病的共同遗传特征

Zhang, Yifan; Liu, Jianfeng; Basang, Zhuoma; Yang, Qianxun; Chen, Hongce; Chen, Shuo; Li, Shaogang; Lei, Changgui; Fang, Mingyan; Liu, Huanhuan; Jin, Xin; Wang, Yingying

Post-transcriptional regulation supports the homeostatic expression of mature RNA

转录后调控支持成熟RNA的稳态表达

Su, Zheng; Fang, Mingyan; Smolnikov, Andrei; Vafaee, Fatemeh; Dinger, Marcel E; Oates, Emily C

INDELpred: Improving the prediction and interpretation of indel pathogenicity within the clinical genome

INDELpred:改进临床基因组中插入缺失致病性的预测和解读

Wei, Yilin; Zhang, Tongda; Wang, Bangyao; Jiang, Xiaosen; Ling, Fei; Fang, Mingyan; Jin, Xin; Bai, Yong

CMDB: the comprehensive population genome variation database of China

CMDB:中国综合人群基因组变异数据库

Li, Zhichao; Jiang, Xiaosen; Fang, Mingyan; Bai, Yong; Liu, Siyang; Huang, Shujia; Jin, Xin