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2014DFB30030

Funded outputs count: 20
Funder award ID: 2014DFB30030
OpenAlex ID: G7394708564
Transcriptome sequencing of hepatocellular carcinoma uncovers multiple types of dysregulated ncRNAs
2022 · Li Zhang, Chunmei Wang, et al. · Frontiers in Oncology · 6
Single-Cell Analysis of Alternative Splicing and Gene Regulatory Network Reveals Remarkable Expression and Regulation Dynamics During Early Embryonic Development
2021 · Jiwei Chen, Yunjin Li, et al. · Research Square · 1
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A comprehensive rat transcriptome built from large scale RNA-seq-based annotation
2020 · Xiangjun Ji, Peng Li, et al. · Nucleic Acids Research · 29
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Genotype-phenotype correlations of Berardinelli-Seip congenital lipodystrophy and novel candidate genes prediction
2020 · Meng Ren, Jingru Shi, et al. · Orphanet Journal of Rare Diseases · 18
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Comprehensive Identification and Characterization of Human Secretome Based on Integrative Proteomic and Transcriptomic Data
2019 · Geng Chen, Jiwei Chen, et al. · Frontiers in Cell and Developmental Biology · 30
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PlantRegMap: charting functional regulatory maps in plants
2019 · Feng Tian, De-Chang Yang, et al. · Nucleic Acids Research · 1,014
Genotype–Phenotype Association Analysis Reveals New Pathogenic Factors for Osteogenesis Imperfecta Disease
2019 · Jingru Shi, Meng Ren, et al. · Frontiers in Pharmacology · 32
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DNMIVD: DNA methylation interactive visualization database
2019 · Wubin Ding, Jiwei Chen, et al. · Nucleic Acids Research · 165
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Systematically Analyzing the Pathogenic Variations for Acute Intermittent Porphyria
2019 · Yibao Fu, Jinmeng Jia, et al. · Frontiers in Pharmacology · 17
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Five-Feature Model for Developing the Classifier for Synergistic vs. Antagonistic Drug Combinations Built by XGBoost
2019 · Xiangjun Ji, Weida Tong, et al. · Frontiers in Genetics · 64
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RDAD: A Machine Learning System to Support Phenotype-Based Rare Disease Diagnosis
2018 · Jinmeng Jia, Ruiyuan Wang, et al. · Frontiers in Genetics · 49
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Deep Learning-Based Multi-Omics Data Integration Reveals Two Prognostic Subtypes in High-Risk Neuroblastoma
2018 · Li Zhang, Chenkai Lv, et al. · Frontiers in Genetics · 202
iProX: an integrated proteome resource
2018 · Jie Ma, Tao Chen, et al. · Nucleic Acids Research · 1,986
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Whole-exome mutational and transcriptional landscapes of combined hepatocellular cholangiocarcinoma and intrahepatic cholangiocarcinoma reveal molecular diversity
2018 · Zhen-Hao Liu, Bao-Feng Lian, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 71
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The Prediction of Drug-Disease Correlation Based on Gene Expression Data
2018 · Hui Cui, Menghuan Zhang, et al. · BioMed Research International · 14
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PedAM: a database for Pediatric Disease Annotation and Medicine
2017 · Jinmeng Jia, Zhongxin An, et al. · Nucleic Acids Research · 19
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Identifying and Characterizing the Circular RNAs during the Lifespan of Arabidopsis Leaves
2017 · Tengfei Liu, Li Zhang, et al. · Frontiers in Plant Science · 80
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Personalizing Chinese medicine by integrating molecular features of diseases and herb ingredient information: application to acute myeloid leukemia
2017 · Lin Huang, Haichang Li, et al. · Oncotarget · 4
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Error-prone DNA polymerase and oxidative stress increase the incidences of A to G mutations in tumors
2016 · Jiannan Lin, Tieliu Shi · Oncotarget · 5
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Biomolecular Network-Based Synergistic Drug Combination Discovery
2016 · Xiangyi Li, Guangrong Qin, et al. · BioMed Research International · 39
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