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RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.

X. Zhan, Y. Hu, B. Li, G. Abecasis, and D. Liu. Bioinform., 32 (9): 1423-1426 (2016)

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Li Li

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DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.P. Wu, S. Nelson, J. Zhao, C. Jr., Q. Feng, Q. Chen, E. Larson, B. Li, N. Cox, C. Stein and 4 other author(s). J. Am. Medical Informatics Assoc., 28 (7): 1421-1430 (2021)Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer's disease with real-world clinical validation.C. Yan, M. Grabowska, A. Dickson, B. Li, Z. Wen, D. Roden, C. Stein, P. Embí, J. Peterson, Q. Feng and 2 other author(s). npj Digit. Medicine, (2024)A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization.Y. Ji, R. Chen, Q. Wang, Q. Wei, R. Tao, and B. Li. BMC Bioinform., 23 (1): 146 (2022)RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.X. Zhan, Y. Hu, B. Li, G. Abecasis, and D. Liu. Bioinform., 32 (9): 1423-1426 (2016)A gradient-boosting approach for filtering de novo mutations in parent-offspring trios.Y. Liu, B. Li, R. Tan, X. Zhu, and Y. Wang. Bioinform., 30 (13): 1830-1836 (2014)DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data.Y. Jiang, G. Giase, K. Grennan, A. Shieh, Y. Xia, L. Han, Q. Wang, Q. Wei, R. Chen, S. Liu and 4 other author(s). PLoS Comput. Biol., (2020)Cancer driver gene discovery through an integrative genomics approach in a non-parametric Bayesian framework.H. Yang, Q. Wei, X. Zhong, H. Yang, and B. Li. Bioinform., 33 (4): 483-490 (2017)A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.R. Chen, Q. Wei, X. Zhan, X. Zhong, J. Sutcliffe, N. Cox, E. Jr., C. Li, W. Chen, and B. Li. Bioinform., 31 (9): 1452-1459 (2015)TVAR: assessing tissue-specific functional effects of non-coding variants with deep learning.H. Yang, R. Chen, Q. Wang, Q. Wei, Y. Ji, X. Zhong, and B. Li. Bioinform., 38 (20): 4697-4704 (October 2022)A computational framework to unify orthogonal information in DNA methylation and copy number aberrations in cell-free DNA for early cancer detection.Q. Wei, C. Jin, Y. Wang, S. Guo, X. Guo, X. Liu, J. An, J. Xing, and B. Li. Briefings Bioinform., (2022)

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Disambiguation of "Li, Bingshan"

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RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.

Please choose a person to relate this publication to

Li Li

Li Li

Li Li

Li Li

Li Li

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Li, Bingshan"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.

Please choose a person to relate this publication to

Li Li

Li Li

Li Li

Li Li

Li Li

Other publications of authors with the same name

Disambiguation

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RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.