Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy von Na, Ji-Hoon, Shin, Saeam, Yang, Donghwa, Kim, Borahm, Kim, Heung Dong, Kim, Sehee, Lee, Joon-Soo, Choi, Jong-Rak, Lee, Seung-Tae, Kang, Hoon-Chul

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Validation and optimization of the Ion Torrent S5 XL sequencer and Oncomine workflow for BRCA1 and BRCA2 genetic testing von Shin, Saeam, Kim, Yoonjung, Chul Oh, Seoung, Yu, Nae, Lee, Seung-Tae, Rak Choi, Jong, Lee, Kyung-A

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Genetic Analysis and Clinical Characteristics of Hereditary Pheochromocytoma and Paraganglioma Syndrome in Korean Population von Choi, Heewon, Kim, Kyoung Jin, Hong, Namki, Shin, Saeam, Choi, Jong-Rak, Kang, Sang Wook, Lee, Seung Tae, Rhee, Yumie

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Evaluation of autoimmune liver disease antibodies in hepatitis patients von Kim, Namsoo, Kim, Sinyoung, Choi, Jong Rak, Park, Younhee

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Klebsiella pneumoniae, a human-dog shuttle organism for the genes of CTX-M ESBL von Yoon, Eun-Jeong, Choi, You Jeong, Won, Dongju, Choi, Jong Rak, Jeong, Seok Hoon

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Comparison of exon-level copy number variants in CytoScan XON assay and next-generation sequencing in clinical samples von Won, Dongju, Yeom, Eunju, Shin, Saeam, Lee, Seung‑Tae, Rak Choi, Jong

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Copy‐number analysis by base‐level normalization: An intuitive visualization tool for evaluating copy number variations von Kim, Hongkyung, Shim, Yeeun, Lee, Taek Gyu, Won, Dongju, Choi, Jong Rak, Shin, Saeam, Lee, Seung‐Tae

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Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy von Kim, Se Hee, Seo, Jieun, Kwon, Soon Sung, Teng, Lip‐Yuen, Won, DongJu, Shin, Saeam, Lee, Joon Soo, Lee, Seung‐Tae, Choi, Jong Rak, Kang, Hoon‐Chul

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Real-World Clinical Utility of Targeted RNA Sequencing in Leukemia Diagnosis and Management von Kim, Seo Wan, Kim, Namsoo, Choi, Yu Jeong, Lee, Seung-Tae, Choi, Jong Rak, Shin, Saeam

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Oxidative status in iron-deficiency anemia von Yoo, Jong-Ha, Maeng, Ho-Young, Sun, Young-Kyu, Kim, Young-Ah, Park, Dong-Wook, Park, Tae Sung, Lee, Seung Tae, Choi, Jong-Rak

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Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy von Kim, Borahm, Won, Dongju, Lee, Seung-Tae, Choi, Jong Rak

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Whole exome sequencing identifies mutational signatures of vitreoretinal lymphoma von Lee, Junwon, Kim, Borahm, Lee, Hyeonah, Park, Heejung, Byeon, Suk Ho, Choi, Jong Rak, Lee, Sung Chul, Lee, Seung-Tae, Lee, Christopher Seungkyu

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Disparate treatment outcomes according to presence of pathogenic mutations in West syndrome von Choi, Han Som, Ko, Ara, Kim, Se Hee, Lee, Seung‐Tae, Choi, Jong Rak, Lee, Joon Soo, Kim, Heung Dong, Kang, Hoon‐Chul

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Real‐world data on prognostic value of measurable residual disease assessment by fragment analysis or next‐generation sequencing in multiple myeloma von Cho, Hyunsoo, Shin, Saeam, Chung, Haerim, Jang, Ji Eun, Kim, Yu Ri, Cheong, June‐Won, Min, Yoo Hong, Lee, Seung‐Tae, Choi, Jong Rak, Kim, Jin Seok

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Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing von Lee, Hyeonah, Seo, Jieun, Shin, Saeam, Lee, Seung-Tae, Choi, Jong Rak

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Clinical relevance of clonal hematopoiesis and its interference in cell-free DNA profiling of patients with gastric cancer von Lee, Kwang Seob, Lee, Choong-Kun, Kwon, Soon Sung, Kwon, Woo Sun, Park, Sejung, Lee, Seung-Tae, Choi, Jong Rak, Rha, Sun Young, Shin, Saeam

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Genetic diagnosis of inborn errors of immunity using clinical exome sequencing von Kwon, Soon Sung, Cho, Youn Keong, Hahn, Seungmin, Oh, Jiyoung, Won, Dongju, Shin, Saeam, Kang, Ji-Man, Ahn, Jong Gyun, Lee, Seung-Tae, Choi, Jong Rak

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Applications of molecular barcode sequencing for the detection of low‐frequency variants in circulating tumour DNA from hepatocellular carcinoma von Lee, Hye Won, Kim, Esl, Cho, Kyung Joo, Park, Hye Jung, Seo, Jieun, Lee, Hyeonah, Baek, Eunha, Choi, Jong Rak, Han, Kwang‐Hyub, Lee, Seung‐Tae, Park, Jun Yong

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Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort von Moon, Dabin, Park, Hye Won, Surl, Dongheon, Won, Dongju, Lee, Seung-Tae, Shin, Saeam, Choi, Jong Rak, Han, Jinu

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Enhancing mutation detection in multiple myeloma with an error-corrected ultra-sensitive NGS assay without plasma cell enrichment von Kim, Jin Ju, Kim, Soo-Jeong, Lim, Seoyoung, Lee, Seung-Tae, Choi, Jong Rak, Shin, Saeam, Hwang, Doh Yu

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