Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sungkyu Kyung"'
Autor:
Jongsuk Chung, Ki-Wook Lee, Chung Lee, Seung-Ho Shin, Sungkyu Kyung, Hyo-Jeong Jeon, Sook-Young Kim, Eunjung Cho, Chang Eun Yoo, Dae-Soon Son, Woong-Yang Park, Donghyun Park
Publikováno v:
BMC Genomics, Vol 20, Iss 1, Pp 1-10 (2019)
Abstract Background Target enrichment is a critical component of targeted deep next-generation sequencing for the cost-effective and sensitive detection of mutations, which is predominantly performed by either hybrid selection or PCR. Despite the adv
Externí odkaz:
https://doaj.org/article/f1cdddc3caad491ebad3d3c77e600864
Publikováno v:
Genomics & Informatics, Vol 14, Iss 4, Pp 211-215 (2016)
The alteration of alternative splicing patterns has an effect on the quantification of functional proteins, leading to phenotype variation. The splicing quantitative trait locus (sQTL) is one of the main genetic elements affecting splicing patterns.
Externí odkaz:
https://doaj.org/article/2c11629329c14f689e36a1bf1cda8cef
Autor:
Jin-Ho Kim, Sungkyu Kyung, Boram Lee, Keunchil Park, Hyun-Tae Shin, Yoon-La Choi, Daeun Ryu, Ki-Wook Lee, Joon Seol Bae, Jae Won Yun, Se-Hoon Lee, Donghyun Park, Myung-Ju Ahn, Woong-Yang Park, Nayoung Kim
Publikováno v:
The Journal of Molecular Diagnostics. 22:304-318
Accurate detection of genomic fusions by high-throughput sequencing in clinical samples with inadequate tumor purity and formalin-fixed, paraffin-embedded tissue is an essential task in precise oncology. We developed the fusion detection algorithm Ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b24fe2a49ec0eb17ed6a45f7e57a5c2
https://doi.org/10.1016/j.jmoldx.2019.10.015
https://doi.org/10.1016/j.jmoldx.2019.10.015
Autor:
Jang-il Sohn, Min-Hak Choi, Dohun Yi, Vipin A. Menon, Yeon Jeong Kim, Junehawk Lee, Jung Woo Park, Sungkyu Kyung, Seung-Ho Shin, Byunggook Na, Je-Gun Joung, Young Seok Ju, Min Sun Yeom, Youngil Koh, Sung-Soo Yoon, Daehyun Baek, Tae-Min Kim, Jin-Wu Nam
Publikováno v:
Nature biomedical engineering.
Variant callers typically produce massive numbers of false positives for structural variations, such as cancer-relevant copy-number alterations and fusion genes resulting from genome rearrangements. Here we describe an ultrafast and accurate detector
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbd5e4c689e663433873a140ae16ca80
https://pubmed.ncbi.nlm.nih.gov/36536253
https://pubmed.ncbi.nlm.nih.gov/36536253
Autor:
Youngil Koh, Daehyun Baek, Je-Gun Joung, Min Hak Choi, Sungkyu Kyung, Tae Min Kim, Jin Wu Nam, Sungro Yoon, Dohun Yi, A. Vipin Menon, Seung-Ho Shin, Byunggook Na, Jang-il Sohn, Yeon Jeong Kim
Genome rearrangements often result in copy number alterations of cancer-related genes and cause the formation of cancer-related fusion genes. Current structural variation (SV) callers, however, still produce massive numbers of false positives (FPs) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59d9b56024aefba34ef610bbad42d9e4
https://doi.org/10.1101/2020.10.25.354456
https://doi.org/10.1101/2020.10.25.354456
Autor:
Ki Woong Sung, Woong-Yang Park, Soo Hyun Lee, Jung-Sun Kim, Keon Hee Yoo, Ji Won Lee, Siyuan Zheng, Joon Seol Bae, Jason T. Huse, Hong Hoe Koo, Sungkyu Kyung
Publikováno v:
Oncotarget
// Soo Hyun Lee 1, 2, * , Jung-Sun Kim 3, * , Siyuan Zheng 4 , Jason T. Huse 2 , Joon Seol Bae 1 , Ji Won Lee 5 , Keon Hee Yoo 5 , Hong Hoe Koo 5 , Sungkyu Kyung 6 , Woong-Yang Park 1, 7 and Ki W. Sung 5 1 Samsung Genome Institute, Samsung Medical Ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b8e2184286e0a64ef57acfd76ff97fb
http://europepmc.org/articles/PMC5542239
http://europepmc.org/articles/PMC5542239
Autor:
Hyun-Tae, Shin, Nayoung K D, Kim, Jae Won, Yun, Boram, Lee, Sungkyu, Kyung, Ki-Wook, Lee, Daeun, Ryu, Jinho, Kim, Joon Seol, Bae, Donghyun, Park, Yoon-La, Choi, Se-Hoon, Lee, Myung-Ju, Ahn, Keunchil, Park, Woong-Yang, Park
Publikováno v:
The Journal of molecular diagnostics : JMD. 22(3)
Accurate detection of genomic fusions by high-throughput sequencing in clinical samples with inadequate tumor purity and formalin-fixed, paraffin-embedded tissue is an essential task in precise oncology. We developed the fusion detection algorithm Ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::242192e9f3480eda9ad532e106ed1291
https://pubmed.ncbi.nlm.nih.gov/31881333
https://pubmed.ncbi.nlm.nih.gov/31881333
Autor:
Eun-Jung Cho, Chang Eun Yoo, Hyo-Jeong Jeon, Dae-Soon Son, Ki-Wook Lee, Woong-Yang Park, Sungkyu Kyung, Jongsuk Chung, Seung-Ho Shin, Sook-Young Kim, Chung Lee, Donghyun Park
Publikováno v:
BMC Genomics
BMC Genomics, Vol 20, Iss 1, Pp 1-10 (2019)
BMC Genomics, Vol 20, Iss 1, Pp 1-10 (2019)
Background Target enrichment is a critical component of targeted deep next-generation sequencing for the cost-effective and sensitive detection of mutations, which is predominantly performed by either hybrid selection or PCR. Despite the advantages o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba264685e508f919147638861f74ce0b
https://doi.org/10.1186/s12864-019-5583-7
https://doi.org/10.1186/s12864-019-5583-7
Publikováno v:
Genomics & Informatics. 14:211
The alteration of alternative splicing patterns has an effect on the quantification of functional proteins, leading to phenotype variation. The splicing quantitative trait locus (sQTL) is one of the main genetic elements affecting splicing patterns.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20b4fd296ec68334d7939ce7adb0e2c5
https://doi.org/10.5808/gi.2016.14.4.211
https://doi.org/10.5808/gi.2016.14.4.211