Author

C. Murray

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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Biochemistry· 1 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

A. Botnar· 1 shared A. P. Piedade· 1 shared A. P. Rochford· 1 shared A. Pashkova· 1 shared A. Vantaux· 1 shared B. Witkowski· 1 shared C. Bourges· 1 shared C. Palmer-Jones· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperMicrobiology

A. Botnar

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Paradigm shift in biomarker translation: a pipeline to generate clinical grade biomarker candidates from DIA-MS discovery

Q. Fu, M. Vegesna, N. Sundararaman, E. Damoc, T. N. Arrey, A. Pashkova, E. Mengesha, P. Debbas, S. Joung, D. Li, S. Cheng, J. Braun, D. P. B. McGovern, C. Murray, Y. Xuan, J. E. Van Eyk

This paper introduces TEAQ, a software tool that selects clinical-grade biomarker candidates from DIA-MS data by evaluating protein quantification metrics in a discovery cohort.

bioRxiv · Mar 20, 2024 · PreprintBiochemistry

A disease-associated gene desert orchestrates macrophage inflammatory responses via ETS2

C. T. Stankey, C. Bourges, T. Turner-Stokes, A. P. Piedade, C. Palmer-Jones, I. Papa, M. Silva dos Santos, L. O. Randzavola, L. Speidel, E. C. Parkes, W. Edwards, A. P. Rochford, C. Murray, J. I. MacRae, P. Skoglund, , J. C. Lee

The paper identifies ETS2 as a master regulator of macrophage inflammatory responses linked to a disease-associated gene desert and shows how modulating this pathway could improve treatment of inflammatory diseases.

bioRxiv · May 5, 2023Immunology

Alkyne modified purines for assessing activation of Plasmodium vivax hypnozoites and growth of pre-erythrocytic and erythrocytic stages in Plasmodium spp.

A. Botnar, G. Lawrence, S. P. Maher, A. Vantaux, B. Witkowski, J. C. Shiau, E. F. Merino, D. De Vore, C. Yang, C. Murray, M. B. Cassera, J. W. Leahy, D. E. Kyle

This study develops alkyne-modified purines as a DNA synthesis marker to distinguish replicating and non-replicating Plasmodium stages, aiding in understanding dormancy mechanisms.

bioRxiv · Oct 12, 2021 · PreprintMicrobiology