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Last updated: 10/9/2026
We design statistically principled methods, develop user-friendly software, and study the genetic basis of human diseases. We currently focus on integrative analysis of genetics and functional genomics data. Topics of interest include:
Mapping disease-critical cellular contexts through integrating GWAS with functional genomics, including scRNA-seq (Turcan 2026 medRxiv, Zhang*,Hou* 2022 Nat Genet), scATAC-seq, and spatial transcriptomics (Yasumizu 2024 Cell Rep).
Resolving target genes and cell types at GWAS loci through integrating regulatory functional data, including building graph foundation models (Huang 2024 in revision at Nat Genet), TWAS fine-mapping (Strober 2025 Nat Genet), and analyzing case-control scRNA-seq data with causal inference.
Understanding the genetic architecture of human diseases and the underlying evolutionary driving forces through analyzing biobank-scale genetics data and functional data (Zhang 2026 Nat Genet).
Building multi-agent systems for automatic computational biology research (See Turcan et al. 2026 ICLR).
We also develop general statistical and machine learning algorithms motivated by applications in genetics; topics include multiple hypotheses testing, multi-armed bandits, dimensionality reduction, empirical Bayes, and causal inference.
Ana's abstract "Calibrated and accurate inference of cell type-specific enhancer-gene links from single-cell multiome data" selected for a talk at 2026 CSHL Biological Data Science Meeting (rate 20%).
9/10/2026Martin received the A. Nico Habermann Career Development Professorship in Computer Science
8/23/2026Preprint "Conditional polygenic enrichment distinguishes causal from tagging disease-critical cell populations in single-cell RNA-seq".