Bingshan Li

Orcid: 0000-0003-2129-168X

According to our database1, Bingshan Li authored at least 16 papers between 2014 and 2024.

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

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

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

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


  Loading...