Author

Michelle Pugh

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· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Ángela SantonjaiD· 1 shared Carlos CaldasiD· 1 shared Elena ProvenzanoiD· 1 shared Emilio AlbaiD· 1 shared Eun Yoon ChoiD· 1 shared Federico RojoiD· 1 shared Harry CliffordiD· 1 shared Helen A. BardwelliD· 1 shared

Activity by Year

2018-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Ángela SantonjaORCID

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1 paper

Recent·Most cited

Shallow whole genome sequencing for robust copy number profiling of formalin-fixed paraffin-embedded breast cancers

Suet‐Feung Chin, Ángela Santonja, Marta Grzelak, Soomin Ahn, Stephen‐John Sammut, Harry Clifford, Oscar M. Rueda, Michelle Pugh, Mae A. Goldgraben, Helen A. Bardwell, Eun Yoon Cho, Elena Provenzano, Federico Rojo, Emilio Alba, Carlos Caldas

This study demonstrates that shallow whole genome sequencing (sWGS) can robustly profile copy number alterations in FFPE breast cancer tissues, even with low-quality DNA.

Experimental and Molecular Pathology · Mar 30, 2018Peer-reviewedGenomics