Literature DB >> 19587683

A highly annotated whole-genome sequence of a Korean individual.

Jong-Il Kim1, 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.   

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 (27.8x 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.

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Year:  2009        PMID: 19587683      PMCID: PMC2860965          DOI: 10.1038/nature08211

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  20 in total

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Journal:  Trends Genet       Date:  2002-11       Impact factor: 11.639

2.  The complete genome of an individual by massively parallel DNA sequencing.

Authors:  David A Wheeler; Maithreyan Srinivasan; Michael Egholm; Yufeng Shen; Lei Chen; Amy McGuire; Wen He; Yi-Ju Chen; Vinod Makhijani; G Thomas Roth; Xavier Gomes; Karrie Tartaro; Faheem Niazi; Cynthia L Turcotte; Gerard P Irzyk; James R Lupski; Craig Chinault; Xing-zhi Song; Yue Liu; Ye Yuan; Lynne Nazareth; Xiang Qin; Donna M Muzny; Marcel Margulies; George M Weinstock; Richard A Gibbs; Jonathan M Rothberg
Journal:  Nature       Date:  2008-04-17       Impact factor: 49.962

3.  Management of High-Throughput DNA Sequencing Projects: Alpheus.

Authors:  Neil A Miller; Stephen F Kingsmore; Andrew Farmer; Raymond J Langley; Joann Mudge; John A Crow; Alvaro J Gonzalez; Faye D Schilkey; Ryan J Kim; Jennifer van Velkinburgh; Gregory D May; C Forrest Black; M Kathy Myers; John P Utsey; Nicholas S Frost; David J Sugarbaker; Raphael Bueno; Stephen R Gullans; Susan M Baxter; Steve W Day; Ernest F Retzel
Journal:  J Comput Sci Syst Biol       Date:  2008-12-26

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Journal:  Nat Genet       Date:  2006-01-29       Impact factor: 38.330

5.  Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations.

Authors:  Hye-Soon Lee; Benjamin D Korman; Julie M Le; Daniel L Kastner; Elaine F Remmers; Peter K Gregersen; Sang-Cheol Bae
Journal:  Arthritis Rheum       Date:  2009-02

6.  Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases.

Authors:  Alexey S Kondrashov
Journal:  Hum Mutat       Date:  2003-01       Impact factor: 4.878

7.  Transcriptome sequencing of malignant pleural mesothelioma tumors.

Authors:  David J Sugarbaker; William G Richards; Gavin J Gordon; Lingsheng Dong; Assunta De Rienzo; Gautam Maulik; Jonathan N Glickman; Lucian R Chirieac; Mor-Li Hartman; Bruce E Taillon; Lei Du; Pascal Bouffard; Stephen F Kingsmore; Neil A Miller; Andrew D Farmer; Roderick V Jensen; Steven R Gullans; Raphael Bueno
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-26       Impact factor: 11.205

8.  DNA loss and evolution of genome size in Drosophila.

Authors:  Dmitri A Petrov
Journal:  Genetica       Date:  2002-05       Impact factor: 1.082

9.  The diploid genome sequence of an individual human.

Authors:  Samuel Levy; Granger Sutton; Pauline C Ng; Lars Feuk; Aaron L Halpern; Brian P Walenz; Nelson Axelrod; Jiaqi Huang; Ewen F Kirkness; Gennady Denisov; Yuan Lin; Jeffrey R MacDonald; Andy Wing Chun Pang; Mary Shago; Timothy B Stockwell; Alexia Tsiamouri; Vineet Bafna; Vikas Bansal; Saul A Kravitz; Dana A Busam; Karen Y Beeson; Tina C McIntosh; Karin A Remington; Josep F Abril; John Gill; Jon Borman; Yu-Hui Rogers; Marvin E Frazier; Stephen W Scherer; Robert L Strausberg; J Craig Venter
Journal:  PLoS Biol       Date:  2007-09-04       Impact factor: 8.029

10.  Genomic convergence analysis of schizophrenia: mRNA sequencing reveals altered synaptic vesicular transport in post-mortem cerebellum.

Authors:  Joann Mudge; Neil A Miller; Irina Khrebtukova; Ingrid E Lindquist; Gregory D May; Jim J Huntley; Shujun Luo; Lu Zhang; Jennifer C van Velkinburgh; Andrew D Farmer; Sharon Lewis; William D Beavis; Faye D Schilkey; Selene M Virk; C Forrest Black; M Kathy Myers; Lar C Mader; Ray J Langley; John P Utsey; Ryan W Kim; Rosalinda C Roberts; Sat Kirpal Khalsa; Meredith Garcia; Victoria Ambriz-Griffith; Richard Harlan; Wendy Czika; Stanton Martin; Russell D Wolfinger; Nora I Perrone-Bizzozero; Gary P Schroth; Stephen F Kingsmore
Journal:  PLoS One       Date:  2008-11-05       Impact factor: 3.240

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  177 in total

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Authors:  Laura E MacConaill; Paul Van Hummelen; Matthew Meyerson; William C Hahn
Journal:  Cancer Discov       Date:  2011-09       Impact factor: 39.397

2.  Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing.

Authors:  Joke Reumers; Peter De Rijk; Hui Zhao; Anthony Liekens; Dominiek Smeets; John Cleary; Peter Van Loo; Maarten Van Den Bossche; Kirsten Catthoor; Bernard Sabbe; Evelyn Despierre; Ignace Vergote; Brian Hilbush; Diether Lambrechts; Jurgen Del-Favero
Journal:  Nat Biotechnol       Date:  2011-12-18       Impact factor: 54.908

3.  Similarity-based disease risk assessment for personal genomes: proof of concept.

Authors:  Jung Hoon Woo; Albert M Lai; Wendy K Chung; Chunhua Weng
Journal:  AMIA Annu Symp Proc       Date:  2011-10-22

4.  Clan genomics and the complex architecture of human disease.

Authors:  James R Lupski; John W Belmont; Eric Boerwinkle; Richard A Gibbs
Journal:  Cell       Date:  2011-09-30       Impact factor: 41.582

Review 5.  Small insertions and deletions (INDELs) in human genomes.

Authors:  Julienne M Mullaney; Ryan E Mills; W Stephen Pittard; Scott E Devine
Journal:  Hum Mol Genet       Date:  2010-09-21       Impact factor: 6.150

6.  Clinical assessment incorporating a personal genome.

Authors:  Euan A Ashley; Atul J Butte; Matthew T Wheeler; Rong Chen; Teri E Klein; Frederick E Dewey; Joel T Dudley; Kelly E Ormond; Aleksandra Pavlovic; Alexander A Morgan; Dmitry Pushkarev; Norma F Neff; Louanne Hudgins; Li Gong; Laura M Hodges; Dorit S Berlin; Caroline F Thorn; Katrin Sangkuhl; Joan M Hebert; Mark Woon; Hersh Sagreiya; Ryan Whaley; Joshua W Knowles; Michael F Chou; Joseph V Thakuria; Abraham M Rosenbaum; Alexander Wait Zaranek; George M Church; Henry T Greely; Stephen R Quake; Russ B Altman
Journal:  Lancet       Date:  2010-05-01       Impact factor: 79.321

7.  Human genome at ten: The sequence explosion.

Authors: 
Journal:  Nature       Date:  2010-04-01       Impact factor: 49.962

8.  Assembly of large genomes using second-generation sequencing.

Authors:  Michael C Schatz; Arthur L Delcher; Steven L Salzberg
Journal:  Genome Res       Date:  2010-05-27       Impact factor: 9.043

9.  CYP2C19 activity comparison between Swedes and Koreans: effect of genotype, sex, oral contraceptive use, and smoking.

Authors:  Margareta Ramsjö; Eleni Aklillu; Lilleba Bohman; Magnus Ingelman-Sundberg; Hyung-Keun Roh; Leif Bertilsson
Journal:  Eur J Clin Pharmacol       Date:  2010-05-25       Impact factor: 2.953

10.  RNA2DNAlign: nucleotide resolution allele asymmetries through quantitative assessment of RNA and DNA paired sequencing data.

Authors:  Mercedeh Movassagh; Nawaf Alomran; Prakriti Mudvari; Merve Dede; Cem Dede; Kamran Kowsari; Paula Restrepo; Edmund Cauley; Sonali Bahl; Muzi Li; Wesley Waterhouse; Krasimira Tsaneva-Atanasova; Nathan Edwards; Anelia Horvath
Journal:  Nucleic Acids Res       Date:  2016-08-30       Impact factor: 16.971

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