Demo Data from EDBT 2026 / reviewers in the wild / expert
Xue Zou
dblp:250/7056
· DBLP profile ↗
2ranked-venue papers
1as first author
1since 2021 · last 2025
—ORCID · conflict
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 1 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › gene expression analysis › gene expression quantification
allele-specific expression |
0.9 | 1 | 2025 | Bayesian estimation of allele-specific expression in the presence of phasing uncertainty · Bioinform. 2025 |
Bioinformatics and computational biology
genomics |
0.3 | 1 | 2025 | Bayesian estimation of allele-specific expression in the presence of phasing uncertainty · Bioinform. 2025 |
Bioinformatics and computational biology › statistical genetics
genotype-phenotype analysis |
0.3 | 1 | 2025 | Bayesian estimation of allele-specific expression in the presence of phasing uncertainty · Bioinform. 2025 |
Methods — techniques the papers use, named apart from their topics
empirical phasing error rates · 0.9bayesian hierarchical model · 0.9
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | Bayesian estimation of allele-specific expression in the presence of phasing uncertaintyabstractMOTIVATION: Allele-specific expression (ASE) analyses aim to detect imbalanced expression of maternal versus paternal copies of an autosomal gene. Such allelic imbalance can result from a variety of cis-acting causes, including disruptive mutations within one copy of a gene that impact the stability of transcripts, as well as regulatory variants outside the gene that impact transcription initiation. Current methods for ASE estimation suffer from a number of shortcomings, such as relying on only one variant within a gene, assuming perfect phasing information across multiple variants within a gene, or failing to account for alignment biases and possible genotyping errors. RESULTS: We developed BEASTIE, a Bayesian hierarchical model designed for precise ASE quantification at the gene level, based on given genotypes and RNA-Seq data. BEASTIE addresses the complexities of allelic mapping bias, genotyping error, and phasing errors by incorporating empirical phasing error rates derived from Genome-in-a-Bottle individual NA12878. BEASTIE surpasses existing methods in accuracy, especially in scenarios with high phasing errors. This improvement is critical for identifying rare genetic variants often obscured by such errors. Through rigorous validation on simulated data and application to real data from the 1000 Genomes Project, we establish the robustness of BEASTIE. These findings underscore the value of BEASTIE in revealing patterns of ASE across gene sets and pathways. AVAILABILITY AND IMPLEMENTATION: The software is freely available from Github (https://github.com/x811zou/BEASTIE); and Zendo (DOI: 10.5281/zenodo.15062124). Xue Zou, Zachary W. Gomez, Timothy E. Reddy, Andrew S. Allen, William H. Majoros |
Bioinform. | 1 |
| 2019 | Symptom-based patient stratification in mental illness using clinical notes
Myung Woo, Xue Zou, Avee Champaneria, Cecilia Lau, Mohammad Imtiaz Mubbashar, Charlotte Schwarz, Jane P. Gagliardi, Jessica D. Tenenbaum |
J. Biomed. Informatics | 3 |