Renjie Tan

发表

LncRNA2Function: a comprehensive resource for functional investigation of human lncRNAs based on RNA-seq data

Jiajie Peng, Yadong Wang, Qinghua Jiang, 2015, BMC Genomics.

Exposing the Causal Effect of Body Mass Index on the Risk of Type 2 Diabetes Mellitus: A Mendelian Randomization Study

Liang Cheng, Yang Hu, He Zhuang, 2019, Front. Genet..

Disease-driven detection of differential inherited SNP modules from SNP network.

Yun Xiao, Tingting Shao, Chuanxing Li, 2011, Gene.

A gradient-boosting approach for filtering de novo mutations in parent-offspring trios

Yadong Wang, Xiaolin Zhu, Yongzhuang Liu, 2014, Bioinform..

LncRNA2Target: a database for differentially expressed genes after lncRNA knockdown or overexpression

Yadong Wang, Rui Ma, Yu Li, 2014, Nucleic Acids Res..

An Evaluation of Copy Number Variation Detection Tools from Whole‐Exome Sequencing Data

Xiaolin Zhu, Yongzhuang Liu, Hongzhe Guo, 2014, Human mutation.

Analyzing large-scale samples confirms the association between the rs1051730 polymorphism and lung cancer susceptibility

Yadong Wang, Qinghua Jiang, Zhijie Han, 2015, Scientific Reports.

ERDS-pe: A paired hidden Markov model for copy number variant detection from whole-exome sequencing data

Yadong Wang, Rui Ma, Rongjie Wang, 2016, 2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).

ProbPFP: A Multiple Sequence Alignment Algorithm Combining Partition Function and Hidden Markov Model with Particle Swarm Optimization

Yadong Wang, Nan Wang, Shuilin Jin, 2018, 2018 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).

ProbPFP: a multiple sequence alignment algorithm combining hidden Markov model optimized by particle swarm optimization with partition function

Nan Wang, Yadong Wang, Shuilin Jin, 2019, BMC Bioinformatics.

ERDS-Exome: A Hybrid Approach for Copy Number Variant Detection from Whole-Exome Sequencing Data

Yadong Wang, Rui Ma, Liran Juan, 2020, IEEE/ACM Transactions on Computational Biology and Bioinformatics.

Accurate in silico confirmation of rare copy number variant calls from exome sequencing data using transfer learning

Yufeng Shen, Renjie Tan, 2022, bioRxiv.

Integrated entropy-based approach for analyzing exons and introns in DNA sequences

Yadong Wang, Renjie Tan, Bo Liu, 2019, BMC Bioinformatics.