Xiaowei Zhan

Orcid: 0000-0002-6249-7193

According to our database1, Xiaowei Zhan authored at least 18 papers between 2014 and 2026.

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

Timeline

Legend:

Book  In proceedings  Article  PhD thesis  Dataset  Other 

Links

Online presence:

On csauthors.net:

Bibliography

2026
Deep reflective reasoning in interdependence constrained structured data extraction from clinical notes for digital health.
CoRR, March, 2026

GNN-EGG: Graph neural network explanations via graph generation.
Neurocomputing, 2026

2025
A Generalized Genetic Random Field Method for the Genetic Association Analysis of Sequencing Data.
CoRR, August, 2025

MiCoDe: a web tool for performing microbiome community detection using a Bayesian weighted stochastic block model.
Bioinform., 2025

2024
A critical assessment of using ChatGPT for extracting structured data from clinical notes.
npj Digit. Medicine, 2024

Navigating electronic health record accuracy by examination of sex incongruent conditions.
J. Am. Medical Informatics Assoc., 2024

Large language models enabled multiagent ensemble method for efficient EHR data labeling.
CoRR, 2024

2023
Unsupervised domain adaptation for nuclei segmentation: Adapting from hematoxylin & eosin stained slides to immunohistochemistry stained slides using a curriculum approach.
Comput. Methods Programs Biomed., November, 2023

2022
A Survey of Statistical Methods for Microbiome Data Analysis.
Frontiers Appl. Math. Stat., 2022

2021
Spatial molecular profiling: platforms, applications and analysis tools.
Briefings Bioinform., 2021

2020
VAMPr: VAriant Mapping and Prediction of antibiotic resistance via explainable features and machine learning.
PLoS Comput. Biol., 2020

Seqminer2: an efficient tool to query and retrieve genotypes for statistical genetics analyses from biobank scale sequence dataset.
Bioinform., 2020

2019
DEFOR: depth- and frequency-based somatic copy number alteration detector.
Bioinform., 2019

2016
FMAP: Functional Mapping and Analysis Pipeline for metagenomics and metatranscriptomics studies.
BMC Bioinform., 2016

RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data.
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
RAREMETAL: fast and powerful meta-analysis for rare variants.
Bioinform., 2014


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