ReliableGenome: annotation of genomic regions with high/low variant calling concordance. - Niko Popitsch; WGS500 Consortium; Anna Schuh; Jenny C. Taylor (Bioinform., 2017)

Hierarchical probabilistic models for multiple gene/variant associations based on next-generation sequencing data. - Dimitrios V. Vavoulis; Jenny C. Taylor; Anna Schuh (Bioinform., 2017)

MichelaNglo: sculpting protein views on web pages without coding. - Matteo P. Ferla; Alistair T. Pagnamenta; David R. Damerell; Jenny C. Taylor; Brian D. Marsden (Bioinform., 2020)

Whole-genome sequencing of patients with rare diseases in a national health system. - Ernest Turro; William J. Astle; Karyn Megy; Stefan Gräf; Daniel Greene; Olga Shamardina; Hana Lango Allen; Alba Sanchis-Juan; Mattia Frontini; Chantal Thys; Jonathan Stephens; Rutendo Mapeta; et al. (Nat., 2020)

A statistical approach for tracking clonal dynamics in cancer using longitudinal next-generation sequencing data. - Dimitrios V. Vavoulis; Anthony Cutts; Jenny C. Taylor; Anna Schuh (Bioinform., 2021)

Fragmenstein: predicting protein-ligand structures of compounds derived from known crystallographic fragment hits using a strict conserved-binding-based methodology. - Matteo P. Ferla; Ruben Sanchez-Garcia; Rachael Skyner; Stefan Gahbauer; Jenny C. Taylor; Frank von Delft; Brian D. Marsden; Charlotte M. Deane (J. Cheminformatics, 2025)