Author
Amy D. Willis
University of WashingtonORCID 0000-0002-2802-4317Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
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2019-2026 · peak 4/yrCo-Author Collaboration Network
10 top collaborators · 4 mutual co-author links13 papers
Recent·Most cited
happi: a Hierarchical Approach to Pangenomics Inference
Pauline Trinh, David S. Clausen, Amy D. Willis
happi tests gene enrichment hypotheses while accounting for genome quality in metagenome-assembled genomes.
Genome biology · Sep 29, 2023Peer-reviewedGenomics
Analyzing microbial evolution through gene and genome phylogenies
Sarah Teichman, Michael Lee, Amy D. Willis
The paper introduces an interactive method for analyzing gene-level phylogenies in microbial evolution, enabling visualization and comparison of gene histories across bacterial strains.
Biostatistics · Sep 25, 2023Peer-reviewedBioinformatics
Differences in gut metagenomes between dairy workers and community controls: a cross-sectional study
Pauline Trinh, Marilyn C. Roberts, Peter MacGarr Rabinowitz, Amy D. Willis
The paper compares gut metagenomes of dairy workers and community controls to assess antibiotic resistance and pathogen exposure risks.
bioRxiv · May 10, 2023 · PreprintGenomics
Implications of taxonomic bias for microbial differential-abundance analysis
Michael R. McLaren, Jacob T. Nearing, Amy D. Willis, Karen G. Lloyd, Benjamin J. Callahan
The paper examines how taxonomic bias affects differential-abundance analysis in microbiome studies and proposes methods to mitigate its effects.
bioRxiv · Aug 19, 2022 · PreprintBioinformatics
Meta-analysis of metagenomes via machine learning and assembly graphs reveals strain switches in Crohn's disease
Taylor E. Reiter, Luiz C. Irber, Alicia A. Gingrich, Dylan Haynes, N. Tessa Pierce‐Ward, Phillip Brooks, Yosuke Mizutani, Dominik Moritz, Felix Reidl, Amy D. Willis, Blair D. Sullivan, C. Titus Brown
The paper identifies five bacterial strains associated with Crohn's disease using a novel method combining machine learning and assembly graphs for metagenomic analysis.
bioRxiv · Jun 30, 2022 · PreprintBioinformatics
Segment number threshold determines juvenile onset of germline cluster proliferation in Platynereis dumerilii
Emily Kuehn, David S. Clausen, Ryan W. Null, Bria M. Metzger, Amy D. Willis, B. Duygu Özpolat
The paper investigates how segment number thresholds influence germline cluster proliferation and gametogenesis in juvenile Platynereis dumerilii, finding a correlation between growth state and developmental stages.
Journal of Experimental Zoology Part B Molecular and Developmental Evolution · Nov 18, 2021Peer-reviewedDevelopmental Biology
A multi-view model for relative and absolute microbial abundances
Brian D. Williamson, James P. Hughes, Amy D. Willis
The paper proposes a method to estimate absolute microbial abundances using both relative and absolute abundance data, improving accuracy by accounting for detection efficiencies.
Biometrics · May 28, 2021Peer-reviewedGenomics
Gene-level metagenomics identifies genome islands associated with immunotherapy response
Samuel S. Minot, Kevin C. Barry, Caroline Kasman, Jonathan L. Golob, Amy D. Willis
The paper introduces a tool for gene-level metagenomic analysis to identify genomic islands linked to immunotherapy response in microbiome data.
Genome biology · May 5, 2021Peer-reviewedBioinformatics
Estimation of cell lineage trees by maximum-likelihood phylogenetics
Jean Feng, William S. DeWitt, Aaron McKenna, Noah Simon, Amy D. Willis, Frederick A. Matsen IV
This paper introduces a statistical model and method for estimating cell lineage trees using maximum-likelihood phylogenetics, showing improved accuracy over existing methods in simulations and zebrafish development.
The Annals of Applied Statistics · Mar 1, 2021Peer-reviewedBioinformatics
Consistent and correctable bias in metagenomic sequencing measurements
Michael R. McLaren, Amy D. Willis, Benjamin J. Callahan
The paper identifies and corrects systematic bias in metagenomic sequencing by modeling how bias distorts measurements and validating it across different protocols and datasets.
eLife · Sep 9, 2019Peer-reviewedBioinformatics
Clustering co-abundant genes identifies components of the gut microbiome that are reproducibly associated with colorectal cancer and inflammatory bowel disease
Samuel S. Minot, Amy D. Willis
The paper introduces a computational method to cluster microbial genes by co-abundance, identifying reproducible gene groups linked to colorectal cancer and inflammatory bowel disease.
Microbiome · Aug 1, 2019Peer-reviewedBioinformatics