Bingshan Li
Orcid: 0000-0003-2129-168X
According to our database1,
Bingshan Li
authored at least 16 papers
between 2014 and 2024.
Collaborative distances:
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Bibliography
2024
Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer's disease with real-world clinical validation.
npj Digit. Medicine, 2024
2023
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.
Nucleic Acids Res., January, 2023
2022
TVAR: assessing tissue-specific functional effects of non-coding variants with deep learning.
Bioinform., October, 2022
A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization.
BMC Bioinform., 2022
A computational framework to unify orthogonal information in DNA methylation and copy number aberrations in cell-free DNA for early cancer detection.
Briefings Bioinform., 2022
2021
DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.
J. Am. Medical Informatics Assoc., 2021
2020
DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data.
PLoS Comput. Biol., 2020
Ultrasound Image-Based Diagnosis of Cirrhosis with an End-to-End Deep Learning model.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2020
2019
De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.
Bioinform., 2019
2017
Cancer driver gene discovery through an integrative genomics approach in a non-parametric Bayesian framework.
Bioinform., 2017
2016
BMC Bioinform., 2016
RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.
Bioinform., 2016
Bioinform., 2016
2015
Bioinform., 2015
A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
Bioinform., 2015
2014
A gradient-boosting approach for filtering <i>de novo</i> mutations in parent-offspring trios.
Bioinform., 2014