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A highly annotated whole-genome sequence of a Korean individual

  • Jong Il Kim
  • , Young Seok Ju
  • , Hansoo Park
  • , Sheehyun Kim
  • , Seonwook Lee
  • , Jae Hyuk Yi
  • , Joann Mudge
  • , Neil A. Miller
  • , Dongwan Hong
  • , Callum J. Bell
  • , Hye Sun Kim
  • , In Soon Chung
  • , Woo Chung Lee
  • , Ji Sun Lee
  • , Seung Hyun Seo
  • , Ji Young Yun
  • , Hyun Nyun Woo
  • , Heewook Lee
  • , Dongwhan Suh
  • , Seungbok Lee
  • Hyun Jin Kim, Maryam Yavartanoo, Minhye Kwak, Ying Zheng, Mi Kyeong Lee, Hyunjun Park, Jeong Yeon Kim, Omer Gokcumen, Ryan E. Mills, Alexander Wait Zaranek, Joseph Thakuria, Xiaodi Wu, Ryan W. Kim, Jim J. Huntley, Shujun Luo, Gary P. Schroth, Thomas D. Wu, Hyeran Kim, Kap Seok Yang, Woong Yang Park, Hyungtae Kim, George M. Church, Charles Lee, Stephen F. Kingsmore, Jeong Sun Seo
  • Seoul National University
  • Macrogen Inc
  • Psoma Therapeutics, Inc.
  • National Center for Genome Resources
  • Brigham and Women’s Hospital
  • Harvard University
  • Illumina, Inc.
  • Genentech, Inc

Research output: Contribution to journalArticlepeer-review

272 Scopus citations

Abstract

Recent advances in sequencing technologies have initiated an era of personal genome sequences. To date, human genome sequences have been reported for individuals with ancestry in three distinct geographical regions: a Yoruba African, two individuals of northwest European origin, and a person from China. Here we provide a highly annotated, whole-genome sequence for a Korean individual, known as AK1. The genome of AK1 was determined by an exacting, combined approach that included whole-genome shotgun sequencing (27.8× coverage), targeted bacterial artificial chromosome sequencing, and high-resolution comparative genomic hybridization using custom microarrays featuring more than 24 million probes. Alignment to the NCBI reference, a composite of several ethnic clades, disclosed nearly 3.45 million single nucleotide polymorphisms (SNPs), including 10,162 non-synonymous SNPs, and 170,202 deletion or insertion polymorphisms (indels). SNP and indel densities were strongly correlated genome-wide. Applying very conservative criteria yielded highly reliable copy number variants for clinical considerations. Potential medical phenotypes were annotated for non-synonymous SNPs, coding domain indels, and structural variants. The integration of several human whole-genome sequences derived from several ethnic groups will assist in understanding genetic ancestry, migration patterns and population bottlenecks.

Original languageEnglish
Pages (from-to)1011-1015
Number of pages5
JournalNature
Volume460
Issue number7258
DOIs
StatePublished - Aug 20 2009

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