Zhen Miao

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Fred Hutchinson Cancer Center

Seattle, WA USA

I develop statistical and machine learning methods to understand cellular regulation from single-cell, spatial, and sequence data. I am a postdoctoral researcher in the Matsen Lab at Fred Hutch Cancer Center and the Howard Hughes Medical Institute. My current work combines antibody language models with explicit models of mutation and selection to study B-cell receptor evolution.

I received my PhD in Genomics and Computational Biology and my MA in Statistics and Data Science from the University of Pennsylvania in 2024. I worked with Junhyong Kim and Nancy Zhang and continued at Penn as a postdoctoral researcher through 2025.

My research connects models of biological variation with models of how assays measure it:

  • Spatial coordination. CoPro identifies gene programs that vary together across neighboring cells and tissue sections. My recent theory paper studies the population targets, identifiability, and stability of spatial kernel restricted canonical correlation analysis.
  • Chromatin accessibility. Paired-Insertion Counting (PIC) provides consistent quantification of single-nucleus ATAC-seq data. PACS tests the effects of multiple biological factors on accessibility while accounting for incomplete capture.
  • Development and disease. I apply these methods to understand cell-state changes and tissue organization, including kidney development and repair. With collaborators, I helped map the single-cell regulatory landscape of the mouse kidney.

My software is available on GitHub. You can find my CV and publications here.

news

Oct 13, 2026 Our new preprint develops statistical theory for spatial kernel restricted canonical correlation analysis, including population targets, identifiability, and stability.
Apr 21, 2026 Our CoPro preprint is available! CoPro identifies coordinated progression of cell states in spatial transcriptomics. Software.
Mar 14, 2026 I am excited to share that I have started my postdoc in the Matsen Lab at Fred Hutchinson Cancer Center in Seattle! I will be working on building antibody language models.
Jan 5, 2025 PACS is published in Nature Communications! The method supports depth-corrected, multifactor analysis of chromatin accessibility in scATAC-seq data.
Nov 7, 2023 I will be giving a talk at Cold Spring Harbor Lab (CSHL) Single Cell Analysis Meeting at Nov 8-11!
Title: Model-based compound hypothesis testing for snATAC-seq data with PACS

selected publications

2026

  1. Spatial Kernel Restricted Canonical Correlation Analysis: Population Targets, Identifiability, and Stability
    Zhen Miao, Yilong Qu, and Nancy R. Zhang
    arXiv (preprint), 2026
  2. Dissecting the coordinated progression of cell states in spatial transcriptomics with CoPro
    Zhen Miao, Yilong Qu, Sijia Huang, Linshan Laux, Samuel Peters, and 6 more authors
    bioRxiv (preprint), 2026

2025

  1. PACS_illustration.svg
    Depth-corrected multi-factor dissection of chromatin accessibility for scATAC-seq data with PACS
    Zhen Miao, Jianqiao Wang, Kernyu Park, Da Kuang, and Junhyong Kim
    Nature Communications, 2025

2024

  1. F1.large.jpg
    Uniform quantification of single-nucleus ATAC-seq data with Paired-Insertion Counting (PIC) and a model-based insertion rate estimator
    Zhen Miao, and Junhyong Kim
    Nature Methods, 2024

2021

  1. dev_kidney_graph.jpg
    Single cell regulatory landscape of the mouse kidney highlights cellular differentiation programs and disease targets
    Zhen Miao, Michael S Balzer, Ziyuan Ma, Hongbo Liu, Junnan Wu, and 9 more authors
    Nature communications, 2021
  2. 41581_2021_463_Fig1_HTML.webp
    Multi-omics integration in the age of million single-cell data
    Zhen Miao, Benjamin D Humphreys, Andrew P McMahon, and Junhyong Kim
    Nature Reviews Nephrology, 2021