Author

Samantha E. Boyle

University of CambridgeORCID 0000-0002-5801-1525Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Carolin M. SaueriD· 1 shared Florian M. MarkowetziD· 1 shared Geoff MacintyreiD· 1 shared James A.M. HalliD· 1 shared James D. BrentoniD· 1 shared Maria ViasiD· 1 shared Matthew EldridgeiD· 1 shared Thomas Paul BradleyiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperBioinformatics

Carolin M. SauerORCID

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1 paper

Recent·Most cited

BioinformaticsbioRxivPreprintJul 19, 2021

Absolute copy number fitting from shallow whole genome sequencing data

Carolin M. Sauer, Matthew Eldridge, Maria Vias…·James D. Brenton

The paper evaluates tools for estimating absolute copy numbers from shallow whole genome sequencing data and introduces an improved tool called Rascal.

19 citations

whole-genome sequencingstatistical model

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