Wanling Yang

Orcid: 0000-0003-0063-6327

According to our database1, Wanling Yang authored at least 11 papers between 2008 and 2026.

Collaborative distances:

Timeline

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Bibliography

2026
SVhet: towards accurate detection of germline heterozygous deletions using short reads.
BMC Bioinform., December, 2026

OTMODE: an optimal transport theory-based framework for identifying differential features in single-cell multi-omics data.
Bioinform., 2026

2025
A framework for integrating GWAS and single-cell RNA-seq with healthy reference controls to identify disease-associated cells.
Briefings Bioinform., 2025

2019
HLA-IMPUTER: an easy to use web application for HLA imputation and association analysis using population-specific reference panels.
Bioinform., 2019

2016
SRinversion: a tool for detecting short inversions by splitting and re-aligning poorly mapped and unmapped sequencing reads.
Bioinform., 2016

2013
PriVar: a toolkit for prioritizing SNVs and indels from next-generation sequencing data.
Bioinform., 2013

2009
In-depth cDNA Library Sequencing Provides Quantitative Gene Expression Profiling in Cancer Biomarker Discovery.
Genom. Proteom. Bioinform., 2009

Linked region detection using high-density SNP genotype data via the minimum recombinant model of pedigree haplotype inference.
BMC Bioinform., 2009

2008
Finding Alternative Splicing Patterns with Strong Support from expressed Sequences on Individual exons/introns.
J. Bioinform. Comput. Biol., 2008

Identification of linked regions using high-density SNP genotype data in linkage analysis.
Bioinform., 2008

Biomarker Identification for Early Tumor Detection Aided by Bioinformatics Gene Expression Analysis.
Proceedings of the 2008 International Conference on BioMedical Engineering and Informatics, 2008


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