Publications

Nitrosylation of β2-Tubulin Promotes Microtubule Disassembly and Differentiated Cardiomyocyte Beating in Ischemic Mice, Tissue Engineering and Regenerative Medicine

RDscan: A New Method for Improving Germline and Somatic Variant Calling Based on Read Depth Distribution, Journal of Computational Biology

Biomarker LEPRE1 induces pelitinib‑specifc drug responsiveness by regulating ABCG2 expression and tumor transition states in human leukemia and lung cancer, Scientific Reports (2022)

Deep learning model enables the discovery of a novel immunotherapeutic agent regulating the kynurenine pathway, OncoImmunology (2021)

Pan-cancer analysis of whole genomes, Nature (2020)

Butler enables rapid cloud-based analysis of thousands of human genomes, Nature Biotechnology (2020)

Integrated genome sizing (IGS) approach for the parallelization of whole genome analysis, BMC Bioinformatics (2019)

Development of the variant calling algorithm, ADIScan, and its use to estimate discordant sequences between monozygotic twins, Nucleic Acids Research (2018)

Prevalence of Rare Genetic Variations and Their Implications in NGS-data Interpretation, Scientific Reports (2017)

HLAscan: genotyping of the HLA region using next-generation sequencing data, BMC Bioinformatics, BMC Bioinformatics (2017)

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia, BMC Medical Genetics (2017)

Genetic characterization of porcine epidemic diarrhea virus in Korea from 1998 to 2013, Archives of Virology (2015)