Author

N. Craig

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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Microbiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

A. Daniels· 2 shared C. Tait-Burkard· 2 shared S. L. Fletcher· 2 shared A. Kratzel· 1 shared A. Warr· 1 shared C. J. Hastie· 1 shared C. Newman· 1 shared H. E. M. Kerr· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersMicrobiology

A. Daniels

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

One for all - Human kidney Caki-1 cells are highly susceptible to infection with corona- and other respiratory viruses

A. Daniels, S. L. Fletcher, H. E. M. Kerr, A. Kratzel, N. Kriplani, N. Craig, C. J. Hastie, P. Davies, P. Digard, V. Thiel, C. Tait-Burkard

This paper identifies Caki-1 human kidney cells as a highly susceptible model for studying multiple respiratory viruses, including coronaviruses and influenza, offering a versatile platform for cross-virus comparison.

bioRxiv · Oct 25, 2022 · PreprintMicrobiology

Direct lysis RT-qPCR of SARS-CoV-2 in cell culture supernatant allows for fast and accurate quantification of virus, opening a vast array of applications

N. Craig, S. L. Fletcher, A. Daniels, C. Newman, M. O'Shea, A. Warr, C. Tait-Burkard

This paper introduces a direct lysis RT-qPCR method for fast, accurate, and cost-effective quantification of SARS-CoV-2 in cell culture supernatant, enabling high-throughput applications.

bioRxiv · Nov 30, 2021 · PreprintMicrobiology