Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Jin Ok, Yang"'
Autor:
Soobok Joe, Jong-Lyul Park, Jun Kim, Sangok Kim, Ji-Hwan Park, Min-Kyung Yeo, Dongyoon Lee, Jin Ok Yang, Seon-Young Kim
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-14 (2024)
Abstract Background Detecting structural variations (SVs) at the population level using next-generation sequencing (NGS) requires substantial computational resources and processing time. Here, we compared the performances of 11 SV callers: Delly, Man
Externí odkaz:
https://doaj.org/article/15e2918bbaff46fd87acfd97f221b2e1
CanISO: a database of genomic and transcriptomic variations in domestic dog (Canis lupus familiaris)
Autor:
In Seok Yang, Insu Jang, Jin Ok Yang, Jinhyuk Choi, Min-Seo Kim, Ka-Kyung Kim, Byung-Joon Seung, Jae-Ho Cheong, Jung-Hyang Sur, Hojung Nam, Byungwook Lee, Junho Kim, Sangwoo Kim
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-12 (2023)
Abstract Background The domestic dog, Canis lupus familiaris, is a companion animal for humans as well as an animal model in cancer research due to similar spontaneous occurrence of cancers as humans. Despite the social and biological importance of d
Externí odkaz:
https://doaj.org/article/79b86829fd834ed6b7380de75438a87d
Autor:
Jin Ok Yang, Min-Hyuk Choi, Ji-Yong Yoon, Jeong-Ju Lee, Sang Ook Nam, Soo Young Jun, Hyeok Hee Kwon, Sohyun Yun, Su-Jin Jeon, Iksu Byeon, Debasish Halder, Juhyun Kong, Byungwook Lee, Jeehun Lee, Joon-Won Kang, Nam-Soon Kim
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/94c77cbe3dbd4cdfb75bbec167c9aee8
Autor:
Jin Ok Yang, Min-Hyuk Choi, Ji-Yong Yoon, Jeong-Ju Lee, Sang Ook Nam, Soo Young Jun, Hyeok Hee Kwon, Sohyun Yun, Su-Jin Jeon, Iksu Byeon, Debasish Halder, Juhyun Kong, Byungwook Lee, Jeehun Lee, Joon-Won Kang, Nam-Soon Kim
Publikováno v:
Frontiers in Genetics, Vol 11 (2021)
Lennox-Gastaut syndrome (LGS) is a severe type of childhood-onset epilepsy characterized by multiple types of seizures, specific discharges on electroencephalography, and intellectual disability. Most patients with LGS do not respond well to drug tre
Externí odkaz:
https://doaj.org/article/4df0e5abdd6e4bddb23b9e4141472469
Autor:
Jeong Yeon Kim, Hongui Cha, Kyeonghui Kim, Changhwan Sung, Jinhyeon An, Hyoeun Bang, Hyungjoo Kim, Jin Ok Yang, Suhwan Chang, Incheol Shin, Seung-Jae Noh, Inkyung Shin, Dae-Yeon Cho, Se-Hoon Lee, Jung Kyoon Choi
Publikováno v:
Nature Genetics. 55:221-231
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::deed95439a3a2c29253bc00a0e2e78b2
https://doi.org/10.1038/s41588-022-01273-y
https://doi.org/10.1038/s41588-022-01273-y
Autor:
Jeongeun Lee, Jean Lee, Sungwon Jeon, Jeongha Lee, Insu Jang, Jin Ok Yang, Soojin Park, Byungwook Lee, Jinwook Choi, Byung-Ok Choi, Heon Yung Gee, Jaeseong Oh, In-Jin Jang, Sanghyuk Lee, Daehyun Baek, Youngil Koh, Sung-Soo Yoon, Young-Joon Kim, Jong-Hee Chae, Woong-Yang Park, Jong Hwa Bhak, Murim Choi
Publikováno v:
Experimental & Molecular Medicine. 54:1862-1871
Despite substantial advances in disease genetics, studies to date have largely focused on individuals of European descent. This limits further discoveries of novel functional genetic variants in other ethnic groups. To alleviate the paucity of East A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d7789b2e9df543cfb87eef2bcef4745
https://doi.org/10.1038/s12276-022-00871-4
https://doi.org/10.1038/s12276-022-00871-4
Autor:
Jin Ok Yang, Sohyun Hwang, Woo-Yeon Kim, Seong-Jin Park, Sang Cheol Kim, Kiejung Park, Byungwook Lee
Publikováno v:
Genomics & Informatics, Vol 12, Iss 1, Pp 42-47 (2014)
Asian populations contain a variety of ethnic groups that have ethnically specific genetic differences. Ethnic variants may be highly relevant in disease and human differentiation studies. Here, we identified ethnically specific variants and then inv
Externí odkaz:
https://doaj.org/article/acca0f492ab1435a83f1ab2c76dec276
Publikováno v:
BMB Reports, Vol 46, Iss 6, Pp 305-309 (2013)
The determination of relatedness between individuals in afamily is crucial in analysis of common complex diseases. Wepresent a method to infer close inter-familial relationshipsbased on SNP genotyping data and provide the relationshipcoefficient of k
Externí odkaz:
https://doaj.org/article/4541cca454114f75919733ec48128de2
Autor:
Soo Young Jun, Min Hyuk Choi, Su Jin Jeon, Joon Won Kang, Ju-Sik Min, Iksu Byeon, Jeong Ju Lee, Nam-Soon Kim, Ji Yong Yoon, Jin Ok Yang, Yong Jae Lee
Publikováno v:
Genetic Testing and Molecular Biomarkers. 24:54-58
Aim: Lennox-Gastaut syndrome (LGS) is a severe type of childhood-onset epilepsy with multiple types of seizures, specific discharges on electroencephalography, and intellectual disability. However, LGS-related genes are largely unknown. To identify c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3ee61c2f6a9794f8b329afae7f0158a
https://doi.org/10.1089/gtmb.2019.0177
https://doi.org/10.1089/gtmb.2019.0177
Autor:
Jeong-Ju Lee, Debasish Halder, Duk Hyun Sung, Byoung Joon Kim, Sohyun Yun, Su-Jin Jeon, Jin Myoung Seok, Nam-Soon Kim, Jung Kyoon Choi, Eui-Jeon Woo, Ja-Hyun Jang, Jin Ok Yang, Jin Whan Cho, Ji-Yong Yoon, Soo Young Jun
Publikováno v:
Genomics. 113(6)
Hereditary Spastic Paraplegias (HSP) are a group of rare inherited neurological disorders characterized by progressive loss of corticospinal motor-tract function. Numerous patients with HSP remain undiagnosed despite screening for known genetic cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1fa680e5bc1e01fb6b9501858a06a9e
https://pubmed.ncbi.nlm.nih.gov/34715294
https://pubmed.ncbi.nlm.nih.gov/34715294