Author

Seong‐Keun Yoo

Macrogen (South Korea)ORCID 0000-0002-8749-7050Unclaimed 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· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:imputation· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Changhoon KimiD· 2 shared Jong-Yeon ShiniD· 2 shared Belong ChoiD· 1 shared Carlos RobelloiD· 1 shared Chang-Uk Kim· 1 shared Darío Arce· 1 shared Fumihiko MatsudaiD· 1 shared Gabriel IllanesiD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersGenomics

Changhoon KimORCID

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2 papers

Recent·Most cited

Indigenous ancestry and admixture in the Uruguayan population

Lucía Spangenberg, María Inés Fariello, Darío Arce, Gabriel Illanes, Gonzalo Greif, Jong-Yeon Shin, Seong‐Keun Yoo, Jeong‐Sun Seo, Carlos Robello, Changhoon Kim, John Novembre, Mónica Sans, Hugo Naya

The paper uses whole-genome sequencing to analyze indigenous ancestry in Uruguayans, identifying Amerindian genetic heritage and estimating admixture timing.

Frontiers in Genetics · Sep 23, 2021Peer-reviewedGenomics

Whole-genome reference panel of 1,781 Northeast Asians improves imputation accuracy of rare and low-frequency variants

Seong‐Keun Yoo, Chang-Uk Kim, Hie Lim Kim, Sungjae Kim, Jong-Yeon Shin, Namcheol Kim, Joshua Sung Woo Yang, Kwok Wai Lo, Belong Cho, Fumihiko Matsuda, Stephan Christoph Schuster, Changhoon Kim, Jong‐Il Kim, Jeong‐Sun Seo

The paper introduces a whole-genome reference panel of 1,781 Northeast Asians, showing improved imputation accuracy for rare and low-frequency variants compared to existing panels.

Genome Medicine · Oct 22, 2019Peer-reviewedGenomics