Jung J - Search Results

1

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia.

Heo SG, Koh Y, Kim JK, Jung J, Kim HL, Yoon SS, Park JW. Heo SG, et al. Among authors: jung j. BMC Med Genet. 2017 Mar 1;18(1):23. doi: 10.1186/s12881-017-0382-y. BMC Med Genet. 2017. PMID: 28249600 Free PMC article.

2

Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.

Kim KS, Kim GS, Hwang JY, Lee HJ, Park MH, Kim KJ, Jung J, Cha HS, Shin HD, Kang JH, Park EK, Kim TH, Hong JM, Koh JM, Oh B, Kimm K, Kim SY, Lee JY. Kim KS, et al. Among authors: jung j. BMC Med Genet. 2007 Nov 26;8:70. doi: 10.1186/1471-2350-8-70. BMC Med Genet. 2007. PMID: 18036257 Free PMC article.

3

Genetic evidence supports linguistic affinity of Mlabri--a hunter-gatherer group in Thailand.

Xu S, Kangwanpong D, Seielstad M, Srikummool M, Kampuansai J, Jin L; HUGO Pan-Asian SNP Consortium. Xu S, et al. BMC Genet. 2010 Mar 19;11:18. doi: 10.1186/1471-2156-11-18. BMC Genet. 2010. PMID: 20302622 Free PMC article.

4

Gene flow between the Korean peninsula and its neighboring countries.

Jung J, Kang H, Cho YS, Oh JH, Ryu MH, Chung HW, Seo JS, Lee JE, Oh B, Bhak J, Kim HL. Jung J, et al. PLoS One. 2010 Jul 29;5(7):e11855. doi: 10.1371/journal.pone.0011855. PLoS One. 2010. PMID: 20686617 Free PMC article.

5

Identification of close relatives in the HUGO Pan-Asian SNP database.

Yang X, Xu S; HUGO Pan-Asian SNP Consortium; Indian Genome Variation Consortium. Yang X, et al. PLoS One. 2011;6(12):e29502. doi: 10.1371/journal.pone.0029502. Epub 2011 Dec 29. PLoS One. 2011. PMID: 22242128 Free PMC article.

6

HLAscan: genotyping of the HLA region using next-generation sequencing data.

Ka S, Lee S, Hong J, Cho Y, Sung J, Kim HN, Kim HL, Jung J. Ka S, et al. Among authors: jung j. BMC Bioinformatics. 2017 May 12;18(1):258. doi: 10.1186/s12859-017-1671-3. BMC Bioinformatics. 2017. PMID: 28499414 Free PMC article.

7

Development of the variant calling algorithm, ADIScan, and its use to estimate discordant sequences between monozygotic twins.

Cho Y, Lee S, Hong JH, Kim BJ, Hong WY, Jung J, Lee HB, Sung J, Kim HN, Kim HL, Jung J. Cho Y, et al. Among authors: jung j. Nucleic Acids Res. 2018 Sep 6;46(15):e92. doi: 10.1093/nar/gky445. Nucleic Acids Res. 2018. PMID: 29873758 Free PMC article.

8

Integrated genome sizing (IGS) approach for the parallelization of whole genome analysis.

Sona P, Hong JH, Lee S, Kim BJ, Hong WY, Jung J, Kim HN, Kim HL, Christopher D, Herviou L, Im YH, Lee KY, Kim TS, Jung J. Sona P, et al. Among authors: jung j. BMC Bioinformatics. 2018 Dec 3;19(1):462. doi: 10.1186/s12859-018-2499-1. BMC Bioinformatics. 2018. PMID: 30509173 Free PMC article.

9

Pan-cancer analysis of whole genomes.

ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium. ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium. Nature. 2020 Feb;578(7793):82-93. doi: 10.1038/s41586-020-1969-6. Epub 2020 Feb 5. Nature. 2020. PMID: 32025007 Free PMC article.

10

Sex differences in oncogenic mutational processes.

Li CH, Prokopec SD, Sun RX, Yousif F, Schmitz N; PCAWG Tumour Subtypes and Clinical Translation; Boutros PC; PCAWG Consortium. Li CH, et al. Nat Commun. 2020 Aug 28;11(1):4330. doi: 10.1038/s41467-020-17359-2. Nat Commun. 2020. PMID: 32859912 Free PMC article.

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