Author

Ángela Santonja

Instituto de Investigación Biomédica de MálagaORCID 0000-0001-9367-7632Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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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

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 Mae A. GoldgrabeniD· 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

Carlos CaldasORCID

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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