A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies - Xihao Li; Han Chen; Margaret Sunitha Selvaraj; Eric Van Buren; Hufeng Zhou; Yuxuan Wang; Ryan Sun; Zachary R. McCaw; Zhi Yu; Min-Zhi Jiang; Daniel DiCorpo; Sheila M. Gaynor; et al. (Nat. Comput. Sci., 2025)

Unsupervised discovery of phenotype-specific multi-omics networks - W. Jenny Shi; Yonghua Zhuang; Pamela H. Russell; Brian D. Hobbs; Margaret M. Parker; Peter J. Castaldi; Pratyaydipta Rudra; Brian Vestal; Craig P. Hersh; Laura M. Saba; Katerina J. Kechris (Bioinform., 2019)

Radtools: R utilities for smooth navigation of medical image data - Pamela H. Russell; Debashis Ghosh (F1000Research, 2018)

Model based heritability scores for high-throughput sequencing data - Pratyaydipta Rudra; W. Jenny Shi; Brian Vestal; Pamela H. Russell; Aaron Odell; Robin D. Dowell; Richard Radcliffe; Laura M. Saba; Katerina J. Kechris (BMC Bioinform., 2017)

Genome-wide synteny through highly sensitive sequence alignment: Satsuma - Manfred G. Grabherr; Pamela H. Russell; Miriah D. Meyer; Evan Mauceli; Jessica Alföldi; Federica Di Palma; Kerstin Lindblad-Toh (Bioinform., 2010)