Poster Session 2025
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- Amanda N. D. Adams
- Scarlet Au
- Dayakar Badri
- Alexander Chan
- Marina Chen
- Jose Collado
- Deepika Dinesh
- Danyue Dong
- Jiayi Duan
- Guilherme Fahur Bottino
- Jasmine Garcia
- McKenzie Gehris
- Ishika Gupta
- Mariss Haddad
- Anna Happel
- Kayla Hazlett
- Lauren Hutchinson
- Jordan Jensen
- Charles Jo
- María Alejandra Jové
- Tanya Karagiannis
- Younhun Kim
- Jae Sun Kim
- Helle Krogh Pedersen
- Valeria Lugo-Mesa
- Wenjie Ma
- Daniel MacDonald
- Sithija Manage
- Olivia Maurer
- Nicholas Medearis
- Steven Medina
- Maeva Metz
- Xochitl Morgan
- Jacob Nearing
- William Nickols
- Etienne Nzabarushimana
- Askarbek Orakov
- Mustafa Özçam
- Tathabbai Pakalapati
- Audrey Randall
- Yesica Daniela Roa Pinilla
- María Alejandra Rodriguez-Alfonso
- Patrick Rynkiewicz
- Laura Schell
- Jiaxian Shen
- Meghan Short
- Wilhelm Sjöland
- Daniel Sprockett
- Melissa Tran
- Benjamin Tully
- Chahat Upreti
- Akshaya Vasudevan
- Emily Venable
- Jasmine Walsh
- Dongyu Wang
- Kai Wang
- Ya Wang
- Zhongjie Wang
- Yilun Wu
- Ji Youn Yoo
Poster Session 2025
Kernel Regression with Tree-Exploring Aggregations
Presented By: Sithija Manage
The proliferation of high-throughput sequencing technologies has generated vast quantities of gut microbiome data, creating an acute need for statistically sound analytical tools. We introduce Kernel Regression with Tree-Exploring Aggregations (KR TEXAS), a novel multivariate nonparametric kernel regression estimator designed to address key challenges in microbiome data analysis: compositionality, zero-inflation, and appropriate taxonomic aggregation. Unlike traditional approaches that require uniform taxonomic aggregation levels (e.g., genus or species), KR TEXAS autonomously learns optimal aggregation levels across different branches of the phylogenetic tree based on each feature’s predictive importance. The estimator employs L1-penalized multivariate Nadaraya-Watson regression with a specifically parameterized distance metric to assign importance coefficients to aggregated features, effectively handling the high sparsity ($>$70\% zeros) common in microbiome datasets. We demonstrate KR TEXAS’s performance through theoretical guarantees, numerical experiments and an application analyzing the relationship between gut microbiome composition and child iron levels from a randomized control trial of biofortified pearl millet in Mumbai. Our approach provides researchers with a flexible, data-driven method for feature aggregation that respects the hierarchical structure of microbial communities while identifying functionally significant taxa at various taxonomic levels.