Author

Henry Marshall

Wellcome Sanger Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cancer Biology· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:whole-genome sequencing· 3 Research Focus:database / resource· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Approach:Bayesian inference· 1 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

Sam BehjatiiD· 2 shared Adam M. H. Young· 1 shared Ágnes OszláncziiD· 1 shared Ahmet Süreyya RifaioğluiD· 1 shared Alexander Aivazidis· 1 shared Alison F. FederiD· 1 shared Andrew L. TrinhiD· 1 shared Andrew R. J. LawsoniD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersGenomics

Sam BehjatiORCID

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Author profile →

3 papers

Recent·Most cited

A comprehensive atlas of somatic mutation rates and mutational signatures in normal human cells

My H. Pham, Luke M. R. Harvey, Thomas R. W. Oliver, Ellie Dunstone, Andrew R. J. Lawson, Pantelis A. Nicola, Rashesh Sanghvi, Yvette E. Hooks, Emily Mitchell, Georgeina L Jarman, Yichen Wang, Federico Abascal, Hyunchul Jung, Matthew D. C. Neville, Yoshihiro Ishida, , Michael R. Stratton

The paper reports mutation rates and mutational signatures across 53 normal human cell types, revealing variation in mutation accumulation and identifying known and unknown mutational processes.

bioRxiv · Aug 29, 2026 · PreprintGenomics

Ultra-deep duplex sequencing reveals unique features of somatic evolution in the normal tissues of a family with Li-Fraumeni syndrome

Hunter Colegrove, Marianne E. Dubard-Gault, Henry Marshall, Brendan F. Kohrn, Thomas Horace Smith, Zachary K. Norgaard, Fang Yin Lo, Elizabeth K. Schmidt, Jacob E. Higgins, Charles C. Valentine, Desiree A. Marshall, John I. Clark, Eric Quentin Konnick, Jesse J. Salk, Marshall S. Horwitz, , Rosa Ana Risques

Duplex sequencing of a Li-Fraumeni family links germline TP53 p.R181H to higher neutral-region mutagenesis and weaker blood TP53 selection, plus recurrent p.R248Q/W hits across proband tissues.

bioRxiv · Aug 20, 2026 · PreprintCancer Biology✦ In-depth digest

A spatiotemporal cancer cell trajectory underlies glioblastoma heterogeneity

Grant de Jong, Fani Memi, Tannia Gracia, Olga Lazareva, Oliver Gould, Alexander Aivazidis, Manàs Dave, Qianqian Zhang, Melanie P. Jensen, Ahmet Süreyya Rifaioğlu, João Diogo Barros-Silva, Sabine E. Eckert, Di Zhou, Yvette Wood, Elizabeth J. Tuck, , Omer Ali Bayraktar

The paper identifies a spatiotemporal cancer cell trajectory in glioblastoma that explains tumor heterogeneity across regions and subclones.

bioRxiv · May 13, 2025 · PreprintCancer Biology