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Byungjin Hwang
Researcher at Yonsei University
Publications - 21
Citations - 1379
Byungjin Hwang is an academic researcher from Yonsei University. The author has contributed to research in topics: Genome editing & Exome sequencing. The author has an hindex of 8, co-authored 18 publications receiving 841 citations. Previous affiliations of Byungjin Hwang include University of California, San Francisco.
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Journal ArticleDOI
Single-cell RNA sequencing technologies and bioinformatics pipelines
TL;DR: The available scRNA-seq technologies and the strategies available to analyze the large quantities of data produced will impact both basic and medical science, from illuminating drug resistance in cancer to revealing the complex pathways of cell differentiation during development.
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Lineage tracing using a Cas9-deaminase barcoding system targeting endogenous L1 elements.
TL;DR: A genome editing strategy is developed using a cytidine deaminase fused with nickase Cas9 (nCas9) to specifically target endogenous interspersed repeat regions in mammalian cells to create genetic barcodes for fine-resolution mapping.
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Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing.
Jung Ah Kim,Byungjin Hwang,Si Nae Park,Sunghoon Huh,Kyongok Im,Sungbin Choi,Hye Yoon Chung,Joo Ryung Huh,Eul Ju Seo,Je-Hwan Lee,Duhee Bang,Dong Soon Lee +11 more
TL;DR: Collectively, mutational profile and adverse prognostic genes in Korean CLL were different from those of Caucasians, suggesting an ethnic difference, while profile of cytogenetic aberrations was similar to those of Caucasianians.
Journal ArticleDOI
CRISPR-Cap: multiplexed double-stranded DNA enrichment based on the CRISPR system
Jeewon Lee,Hyeonseob Lim,Hoon Jang,Byungjin Hwang,JoonHo Lee,Junhyuk Cho,Ji Hyun Lee,Duhee Bang +7 more
TL;DR: CRISPR-Cap is developed, a simple and scalable CRISpr-based method to enrich target regions of dsDNA, requiring only two short experimental procedures that can be completed within two hours, and can be used as an alternative to other widely used target-enrichment methods, which will broaden the scope of CRISPR applications to the field of target enrichment field.
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Genetic testing of Korean familial hypercholesterolemia using whole-exome sequencing.
Soo Min Han,Byungjin Hwang,Tae Gun Park,Do Il Kim,Moo Yong Rhee,Byoung Kwon Lee,Young Keun Ahn,Byung Ryul Cho,Jeong Taek Woo,Seung Ho Hur,Jin Ok Jeong,Sungha Park,Yangsoo Jang,Min Goo Lee,Duhee Bang,Ji Hyun Lee,Sang Hak Lee +16 more
TL;DR: This study confirmed the utility of genetic diagnosis of FH through WES through whole-exome sequencing and identified three novel causative mutations in Koreans that were validated by co-segregation in their relatives.