Volgen
Renjie Tan
Renjie Tan
Harbin Medical University
Geverifieerd e-mailadres voor hrbmu.edu.cn
Titel
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Geciteerd door
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An evaluation of copy number variation detection tools from whole‐exome sequencing data
R Tan, Y Wang, SE Kleinstein, Y Liu, X Zhu, H Guo, Q Jiang, AS Allen, ...
Human mutation 35 (7), 899-907, 2014
2622014
LncRNA2Function: a comprehensive resource for functional investigation of human lncRNAs based on RNA-seq data
Q Jiang, R Ma, J Wang, X Wu, S Jin, J Peng, R Tan, T Zhang, Y Li, ...
BMC genomics 16, 1-11, 2015
1362015
LncRNA2Target: a database for differentially expressed genes after lncRNA knockdown or overexpression
Q Jiang, J Wang, X Wu, R Ma, T Zhang, S Jin, Z Han, R Tan, J Peng, G Liu, ...
Nucleic acids research 43 (D1), D193-D196, 2015
1292015
Exposing the causal effect of body mass index on the risk of type 2 diabetes mellitus: a mendelian randomization study
L Cheng, H Zhuang, H Ju, S Yang, J Han, R Tan, Y Hu
Frontiers in genetics 10, 431896, 2019
592019
A gradient-boosting approach for filtering de novo mutations in parent–offspring trios
Y Liu, B Li, R Tan, X Zhu, Y Wang
Bioinformatics 30 (13), 1830-1836, 2014
402014
A generalized topological entropy for analyzing the complexity of DNA sequences
S Jin, R Tan, Q Jiang, L Xu, J Peng, Y Wang, Y Wang
PLoS One 9 (2), e88519, 2014
212014
Integrated entropy-based approach for analyzing exons and introns in DNA sequences
J Li, L Zhang, H Li, Y Ping, Q Xu, R Wang, R Tan, Z Wang, B Liu, Y Wang
BMC bioinformatics 20, 1-7, 2019
192019
ProbPFP: a multiple sequence alignment algorithm combining hidden Markov model optimized by particle swarm optimization with partition function
Q Zhan, N Wang, S Jin, R Tan, Q Jiang, Y Wang
BMC bioinformatics 20, 1-10, 2019
152019
Analyzing large-scale samples confirms the association between the rs1051730 polymorphism and lung cancer susceptibility
Z Han, Q Jiang, T Zhang, X Wu, R Ma, J Wang, Y Bai, R Wang, R Tan, ...
Scientific reports 5 (1), 15642, 2015
142015
Disease-driven detection of differential inherited SNP modules from SNP network
C Li, Y Li, J Xu, J Lv, Y Ma, T Shao, B Gong, R Tan, Y Xiao, X Li
Gene 489 (2), 119-129, 2011
112011
Probpfp: A multiple sequence alignment algorithm combining partition function and hidden Markov model with particle swarm optimization
Q Zhan, N Wang, S Jin, R Tan, Q Jiang, Y Wang
2018 IEEE International Conference on Bioinformatics and Biomedicine (BIBM …, 2018
82018
ERDS-exome: a hybrid approach for copy number variant detection from whole-exome sequencing data
R Tan, J Wang, X Wu, L Juan, T Zhang, R Ma, Q Zhan, T Wang, S Jin, ...
IEEE/ACM Transactions on Computational Biology and Bioinformatics 17 (3 …, 2017
62017
Accurate in silico confirmation of rare copy number variant calls from exome sequencing data using transfer learning
R Tan, Y Shen
Nucleic Acids Research 50 (21), e123-e123, 2022
42022
Association of Predicted Damaging De Novo Variants on Ventricular Function in Individuals With Congenital Heart Disease
MJ Lewis, A Hsieh, L Qiao, R Tan, B Kazzi, A Channing, EL Griffin, ...
Circulation: Genomic and Precision Medicine 16 (2), e003900, 2023
22023
ERDS-pe: A paired hidden Markov model for copy number variant detection from whole-exome sequencing data
R Tan, J Wang, X Wu, G Wan, R Wang, R Ma, Z Han, W Zhou, S Jin, ...
2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM …, 2016
22016
The complexity of promoter regions based on a vector topological entropy
S Jin, Z Wang, J Lin, J Wang, X Zhang, R Tan, C Zhang, Z Wang, W Guo, ...
Current Bioinformatics 12 (5), 471-474, 2017
12017
Disease-driven detection of differential inherited SNP modules from SNP network
R Tan, Y Xiao, X Li
2011
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Artikelen 1–17