Author

Rachel J. Spruce

University of BirminghamORCID 0009-0002-8235-2116Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Assay:DNA methylation· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Andrew BlakeiD· 1 shared Andrew David BeggsiD· 1 shared Celina WhalleyiD· 1 shared Enric DomingoiD· 1 shared Hisham Mohamed MehannaiD· 1 shared Jill M. BrooksiD· 1 shared Karl F.B. PayneiD· 1 shared Nikolaos BatisiD· 1 shared

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2021-2021 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andrew BlakeORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineEpigenomesPeer-reviewedFeb 19, 2021

Ultra-low DNA input into whole genome methylation assays and detection of oncogenic methylation & copy number variants in circulating tumour DNA

Celina Whalley, Karl F.B. Payne, Enric Domingo…·Andrew David Beggs

This study demonstrates that the Illumina Infinium HD methylation assay can reliably detect methylation and copy number variants in low-input DNA samples, including circulating tumour DNA.

13 citations

humanDNA methylation

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