Bingshan Li

Orcid: 0000-0003-2129-168X

According to our database1, Bingshan Li authored at least 17 papers between 2014 and 2024.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2024
Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer's disease with real-world clinical validation.
npj Digit. Medicine, 2024

Improving Genetic Perturbation Response Prediction with an Enhanced Biological Knowledge Graph.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 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
A computational method for genotype calling in family-based sequencing data.
BMC Bioinform., 2016

RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.
Bioinform., 2016

Joint detection of copy number variations in parent-offspring trios.
Bioinform., 2016

2015
A Bayesian framework for <i>de novo</i> mutation calling in parents-offspring trios.
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


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