Author

Soomin Ahn

Seoul National UniversityORCID 0000-0002-1979-4010Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Research Focus:phylogenetics / evolution· 1 Assay:whole-exome sequencing· 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 Haesook T. Kim· 1 shared Harry CliffordiD· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenomics

Ángela SantonjaORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Gallbladder adenocarcinomas undergo subclonal diversification and selection from precancerous lesions to metastatic tumors

Min-Su Kang, Hee Young Na, Soomin Ahn, Ji-Won Kim, Ju Hyun Lee, 안소연, Jeonghwan Youk, Haesook T. Kim, Se Hyun Kim, Koung Jin Suh, J Y Lee, Jin Won Kim, Yu Jung Kim, Keun‐Wook Lee, Jong Seok Lee, , Ho‐Seong Han

This study traces the evolutionary paths of gallbladder adenocarcinomas, showing subclonal diversification and selection from precancerous lesions to metastatic tumors.

eLife · Dec 8, 2022Peer-reviewedGenetics

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