According to our database1, Bingshan Li authored at least 8 papers between 2014 and 2019.
Legend:Book In proceedings Article PhD thesis Other
De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.
Cancer driver gene discovery through an integrative genomics approach in a non-parametric Bayesian framework.
A computational method for genotype calling in family-based sequencing data.
BMC Bioinformatics, 2016
RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.
Joint detection of copy number variations in parent-offspring trios.
A Bayesian framework for de novo mutation calling in parents-offspring trios.
A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
A gradient-boosting approach for filtering de novo mutations in parent-offspring trios.