Author

Matthew N. Davies

Institute of Cancer Research

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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Genomics· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Aleruchi Okachi· 1 shared Alfonso Buil· 1 shared Ana Viñuela· 1 shared Andrew A. Brown· 1 shared Andrew Charles WotherspooniD· 1 shared Andrew WoolstoniD· 1 shared Anisha PateliD· 1 shared Antonino ZitoiD· 1 shared

Activity by Year

2016-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperGenomics

Aleruchi Okachi

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3 papers

Recent·Most cited

Heritability of skewed X-inactivation in female twins is tissue-specific and dependent on age

Antonino Zito, Matthew N. Davies, Pei-Chien Tsai, Susanna Roberts, Rosa Andres Ejarque, Stefano Nardone, Jordana T. Bell, Chloe C. Y. Wong, Kerrin S. Small

This study quantifies XCI skewing in female twins across tissues, showing age- and tissue-specific heritability and associations with smoking in older females.

Nature Communications · Nov 25, 2019Peer-reviewedGenetics

Ultra-sensitive mutation detection and genome-wide DNA copy number reconstruction by error corrected circulating tumour DNA sequencing

Sonia Mansukhani, Louise J. Barber, Dimitrios Kleftogiannis, Sing Yu Moorcraft, Michael Davidson, Andrew Woolston, Paula Proszek, Beatrice L. Griffiths, Kerry Fenwick, Bram Herman, Nik Matthews, Ben O’Leary, Sanna Hulkki Wilson, David González de Castro, Anisha Patel, , Marco Gerlinger

This paper develops an error-corrected cfDNA sequencing method for highly sensitive mutation detection and genome-wide copy number reconstruction in metastatic colorectal cancer.

Clinical Chemistry · Aug 27, 2018Peer-reviewedGenomics

Quantifying the degree of sharing of genetic and non-genetic causes of gene expression variability across four tissues.

Alfonso Buil, Ana Viñuela, Andrew A. Brown, Matthew N. Davies, Ismael Padioleau, Deborah Bielser, Luciana Romano, Daniel Glass, Paola Di Meglio, Kerrin S. Small, Timothy D. Spector, Emmanouil T. Dermitzakis

The paper quantifies shared and tissue-specific genetic and non-genetic causes of gene expression variability across four tissues using twin data.

bioRxiv · May 13, 2016 · PreprintGenomics