Author

Stacey Price

Wellcome Sanger Institute

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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Genetics· 1 Genomics· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:CRISPR screen· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Emanuel GonçalvesiD· 2 shared Francesco IorioiD· 2 shared Julio Sáez-RodrígueziD· 2 shared Mathew J. GarnettiD· 2 shared Steven P. WilliamsiD· 2 shared Ultan McDermottiD· 2 shared Alba Dalmases· 1 shared Alessandro VincetiiD· 1 shared

Activity by Year

2017-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenomics

Emanuel GonçalvesORCID

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Author profile →

3 papers

Recent·Most cited

Minimal genome-wide human CRISPR-Cas9 library

Emanuel Gonçalves, Mark Thomas, Fiona M. Behan, Gabriele Picco, Clare Pacini, Felicity R. Allen, Alessandro Vinceti, Mamta Sharma, David A. Jackson, Stacey Price, Charlotte Beaver, Oliver M. Dovey, David J. Parry-Smith, Francesco Iorio, Leopold Parts, , Mathew J. Garnett

The paper designs a smaller genome-wide CRISPR-Cas9 library with reduced size while maintaining sensitivity and specificity, enhancing its applicability in complex models.

Genome biology · Jan 21, 2021Peer-reviewedGenomics

Genomic determinants of protein abundance variation in colorectal cancer cells

Theodoros I. Roumeliotis, Steven P. Williams, Emanuel Gonçalves, Clara Alsinet, Martin Del Castillo Velasco‐Herrera, Nanne Aben, Fatemeh Zamanzad Ghavidel, Magali Michaut, Michaël Schubert, Stacey Price, James C. Wright, Lu Yu, Mi Yang, Rodrigo Dienstmann, Justin Guinney, , Jyoti Sharma Choudhary

The paper quantifies proteomic and genomic variation in colorectal cancer cell lines to understand how mutations affect protein levels and drug responses.

Cell Reports · Aug 1, 2017Peer-reviewedSystems Biology

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, Steven P. Williams, Luz García‐Alonso, Alba Dalmases, Beatríz Bellosillo, Carla Daniela Robles‐Espinoza, Stacey Price, Syd Barthorpe, Patrick S. Tarpey, Constantine Alifrangis, Graham R. Bignell, Joana Vidal, Jamie Young, , 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.

Genome Research · Apr 1, 2017Peer-reviewedGenetics