Author

Patrick S. Tarpey

Wellcome Sanger InstituteORCID 0000-0002-2042-4543Unclaimed ORCID profile · follow to get notified of new preprints

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Patrick S. Tarpey1 paper

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Graham R. Bignell· 2 shared Iñigo MartincorenaiD· 2 shared Ultan McDermottiD· 2 shared Abel DevadassiD· 1 shared Adam M. H. Young· 1 shared Alba Dalmases· 1 shared Alvis BrāzmaiD· 1 shared Beatríz BellosilloiD· 1 shared

Activity by Year

2017-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenomics

Graham R. Bignell

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2 papers

Recent·Most cited

GenomicsScientific ReportsPeer-reviewedSep 4, 2018

An integrated genomic analysis of anaplastic meningioma identifies prognostic molecular signatures

Grace Collord, Patrick S. Tarpey, Natalja Kurbatova…·Ultan McDermott

This study identifies two molecular subgroups of anaplastic meningioma with distinct survival outcomes and links them to specific genetic mutations.

62 citationstop 3%

humanwhole-genome sequencing

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GeneticsGenome ResearchPeer-reviewedApr 1, 2017

Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutations.

Jonathan S. Brammeld, Mia Petljak, Iñigo Martincorena…·Ultan McDermott

This paper describes a method to identify drug resistance mutations in cancer using genome-wide chemical mutagenesis and next-generation sequencing, enabling the discovery of both known and novel resistance mechanisms.

23 citations

humanwhole-genome sequencing

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