Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Myungguen Chung"'
Publikováno v:
Genomics & Informatics, Vol 12, Iss 4, Pp 236-239 (2014)
The genetic regulation of glucose and insulin levels might be modified by adiposity. With regard to the genetic factors that are altered by adiposity, a large meta-analysis on the interactions between genetic variants and body mass index with regard
Externí odkaz:
https://doaj.org/article/7a20ccfa74c445d2ae54e1d750b60418
Publikováno v:
Genomics & Informatics, Vol 12, Iss 4, Pp 187-194 (2014)
Metabolic syndrome (METS) is a disorder of energy utilization and storage and increases the risk of developing cardiovascular disease and diabetes. To identify the genetic risk factors of METS, we carried out a genome-wide association study (GWAS) fo
Externí odkaz:
https://doaj.org/article/2cb023f498a94493b233469420d0232b
Autor:
Sol Moe Lee, Myungguen Chung, Jae Wook Hyeon, Seok Won Jeong, Young Ran Ju, Heebal Kim, Jeongmin Lee, SangYun Kim, Seong Soo A An, Sung Beom Cho, Yeong Seon Lee, Su Yeon Kim
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0157540 (2016)
Inherited prion diseases (IPDs), including genetic Creutzfeldt-Jakob disease (gCJD), account for 10-15% of cases of prion diseases and are associated with several pathogenic mutations, including P102L, V180I, and E200K, in the prion protein gene (PRN
Externí odkaz:
https://doaj.org/article/5ae6c7ca5e134d6d87ac54ad32a1f07a
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e114128 (2014)
Most genome-wide association studies consider genes that are located closest to single nucleotide polymorphisms (SNPs) that are highly significant for those studies. However, the significance of the associations between SNPs and candidate genes has n
Externí odkaz:
https://doaj.org/article/3fe868063d484145a4b1d150b65bb00a
Autor:
Jongpill Choi, Seong Beom Cho, Myungguen Chung, Hyo-Jeong Ban, Hyun Youn Jo, Kyung-Won Hong, Kwang Su Jung
Publikováno v:
Database: The Journal of Biological Databases and Curation
Since 2012, the Center for Genome Science of the Korea National Institute of Health (KNIH) has been sequencing complete genomes of 1722 Korean individuals. As a result, more than 32 million variant sites have been identified, and a large proportion o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::653e19559cd991016c5ed37a93eb2db5
https://pubmed.ncbi.nlm.nih.gov/32133509
https://pubmed.ncbi.nlm.nih.gov/32133509
Publikováno v:
Biomolecules & Therapeutics
We aimed to understand the molecular changes in host cells that accompany infection by the seasonal influenza A H1N1 virus because the initial response rapidly changes owing to the fact that the virus has a robust initial propagation phase. Human epi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8e4361fbfa68a75f7fe5e7afc1480d9
https://pubmed.ncbi.nlm.nih.gov/29401570
https://pubmed.ncbi.nlm.nih.gov/29401570
Autor:
Sol Moe Lee1,2 (AUTHOR), Myungguen Chung3,4 (AUTHOR), Kyu Jam Hwang1 (AUTHOR), Young Ran Ju1 (AUTHOR), Jae Wook Hyeon1 (AUTHOR), Jun-Sun Park1 (AUTHOR), Chi-Kyeong Kim1 (AUTHOR), Sangho Choi1 (AUTHOR), Jeongmin Lee1 (AUTHOR), Su Yeon Kim1 (AUTHOR) tenksy@korea.krq
Publikováno v:
BMC Medical Genomics. 2014, Vol. 7 Issue 1, p52-62. 11p. 4 Diagrams, 1 Chart.
Publikováno v:
Genomics & Informatics, Vol 12, Iss 4, Pp 187-194 (2014)
Genomics & Informatics
Genomics & Informatics
Metabolic syndrome (METS) is a disorder of energy utilization and storage and increases the risk of developing cardiovascular disease and diabetes. To identify the genetic risk factors of METS, we carried out a genome-wide association study (GWAS) fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81afc97121e619aed3eeca58d74ce618
http://genominfo.org/upload/pdf/gni-12-187.pdf
http://genominfo.org/upload/pdf/gni-12-187.pdf
Publikováno v:
BioChip Journal. 7:6-10
In recent genome-wide association studies, the task of genotype imputation for missing SNPs is a common procedure to increase the power of observed genetic markers. For genotype imputation, they usually employ publicly available resources, such as th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afdcbfaf7bb0af43544c7c855f5f1077
https://doi.org/10.1007/s13206-013-7102-2
https://doi.org/10.1007/s13206-013-7102-2
Publikováno v:
BioChip Journal. 7:63-67
This paper addresses the issue of improving long imputation time usually required for a large volume of SNP genotype data which can be easily obtained by biological experiments with the genomewide SNP chip or the next-generation sequencing technology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d00ce0186cc933cfd3546fac1f4579d
https://doi.org/10.1007/s13206-013-7110-2
https://doi.org/10.1007/s13206-013-7110-2