Related Experiment Video

Updated: Jan 5, 2026

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
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Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

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NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency

Seong-Keun Yoo1,2, Chang-Uk Kim2,3, Hie Lim Kim4,5

  • 1Precision Medicine Center, Seoul National University Bundang Hospital, 172 Dolma-ro, Seongnam, Bundang-gu, Gyeonggi-do, 13605, Republic of Korea.

Genome Medicine
|October 24, 2019
PubMed

Keywords:
East AsiansGenotype imputationNortheast AsiansReference panelWhole-genome sequencing

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