Author

A. B. Gill

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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Animal Behavior & Cognition· 1 Bioengineering· 1 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:clustering· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

F. A. Gallagher· 2 shared A. Durrani· 1 shared A. Hermans· 1 shared A. J. Murk· 1 shared A. Marshall· 1 shared A. N. Priest· 1 shared A. Y. Warren· 1 shared C. Alifrangis· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersBioengineering

F. A. Gallagher

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Author profile →

3 papers

Recent·Most cited

Do electromagnetic fields from subsea power cables effect elasmobranch behaviour? A risk-based approach for the Dutch Continental Shelf

A. Hermans, H. V. Winter, A. B. Gill, A. J. Murk

The paper assesses the risk of subsea power cable electromagnetic fields on elasmobranch behavior using modeled exposure levels and sensory sensitivity data.

bioRxiv · Dec 1, 2023 · PreprintAnimal Behavior & Cognition

3D-printed moulds for image-guided surgical biopsies: an open source computational platform

C.-O. Mireia, M. Gehrung, S. Ursprung, A. B. Gill, A. Y. Warren, L. Beer, F. A. Gallagher, T. J. Mitchell, I. A. Mendichovszky, A. N. Priest, G. D. Stewart, E. Sala, F. Markowetz

This paper develops an open-source computational platform to create 3D-printed moulds for image-guided surgical biopsies, achieving accurate co-registration of imaging and tissue samples.

bioRxiv · Mar 4, 2020 · PreprintBioengineering

High-sensitivity monitoring of ctDNA by patient-specific sequencing panels and integration of variant reads

J. C. Wan, K. Heider, D. Gale, S. Murphy, E. Fisher, J. Morris, F. Mouliere, D. Chandrananda, A. Marshall, A. B. Gill, P. Y. Chan, E. Barker, G. Young, W. N. Cooper, I. Hudecova, , N. Rosenfeld

This paper introduces INVAR, a method to improve ctDNA detection sensitivity using patient-specific sequencing panels and variant read integration, achieving ppm-level detection in clinical samples.

bioRxiv · Sep 11, 2019 · PreprintCancer Biology