Browsing by Yonsei Author : Kim, Sangwoo

Kim, Sangwoo [김상우]
Department :
College of Medicine (의과대학) - Dept. of Biomedical Systems Informatics (의생명시스템정보학교실)
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Showing results 1 to 46 of 46

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Issue DateTitleJournal Title
2020Wnt/β-catenin signaling pathway induces autophagy-mediated temozolomide-resistance in human glioblastomaCELL DEATH & DISEASE
2020Cross-species oncogenic signatures of breast cancer in canine mammary tumors NATURE COMMUNICATIONS
2020Prognostic Value of CD200R1 mRNA Expression in Head and Neck Squamous Cell Carcinoma CANCERS
2020Comparison of whole mitochondrial genome variants between hair shafts and reference samples using massively parallel sequencingINTERNATIONAL JOURNAL OF LEGAL MEDICINE
2020Molecular subtypes of oropharyngeal cancer show distinct immune microenvironment related with immune checkpoint blockade response BRITISH JOURNAL OF CANCER
2019Molecular characterization of lung adenocarcinoma from Korean patients using next generation sequencing PLOS ONE
2019BAMixChecker: an automated checkup tool for matched sample pairs in NGS cohort BIOINFORMATICS
2019Impact of mouse contamination in genomic profiling of patient-derived models and best practice for robust analysis GENOME BIOLOGY
2019Whole-exome and whole-transcriptome sequencing of canine mammary gland tumors Scientific Data
2019Investigating the Feasibility of Targeted Next-Generation Sequencing to Guide the Treatment of Head and Neck Squamous Cell Carcinoma Cancer Research and Treatment
2019Characteristic gene alterations in primary gastrointestinal T- and NK-cell lymphomasLEUKEMIA
2019A therapeutic strategy for chemotherapy-resistant gastric cancer via destabilization of both β-catenin and ras CANCERS
2019Molecular Diagnostic Assays and Clinicopathologic Implications of MET Exon 14 Skipping Mutation in Non-small-cell Lung CancerCLINICAL LUNG CANCER
2019The use of technical replication for detection of low-level somatic mutations in next-generation sequencing NATURE COMMUNICATIONS
2018Neopepsee: accurate genome-level prediction of neoantigens by harnessing sequence and amino acid immunogenicity informationANNALS OF ONCOLOGY
2018AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencingBIOINFORMATICS
2018Isoform specific gene expression analysis of KRAS in the prognosis of lung adenocarcinoma patients BMC BIOINFORMATICS
2018Palmitate and minimally-modified low-density lipoprotein cooperatively promote inflammatory responses in macrophages PLOS ONE
2018Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathyEPILEPSY RESEARCH
2017Somatic mutation driven codon transition bias in human cancer SCIENTIFIC REPORTS
2017In Silico Simulation of Signal Cascades in Biomedical Networks Based on the Production Rule SystemLecture Notes in Computer Science
2017Next-generation sequencing reveals novel resistance mechanisms and molecular heterogeneity in EGFR-mutant non-small cell lung cancer with acquired resistance to EGFR-TKIsLUNG CANCER
2017Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical DysplasiaAMERICAN JOURNAL OF HUMAN GENETICS
2016Pilot Study of a Next-Generation Sequencing-Based Targeted Anticancer Therapy in Refractory Solid Tumors at a Korean Institution PLOS ONE
2016Next-generation sequencing reveals somatic mutations that confer exceptional response to everolimus ONCOTARGET
2016Vecuum: identification and filtration of false somatic variants caused by recombinant vector contaminationBIOINFORMATICS
2016ISOexpresso: a web-based platform for isoform-level expression analysis in human cancer BMC GENOMICS
2016Exome sequencing reveals recurrent REV3L mutations in cisplatin-resistant squamous cell carcinoma of head and neck SCIENTIFIC REPORTS
2016Establishment and characterisation of patient-derived xenografts as paraclinical models for gastric cancer SCIENTIFIC REPORTS
2015Analysis of Whole Transcriptome Sequencing Data: Workflow and Software Genomics & Informatics
2015An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development NATURE MEDICINE
2015SoloDel: a probabilistic model for detecting low-frequent somatic deletions from unmatched sequencing dataBIOINFORMATICS
2015Identification of genomic features in the classification of loss- and gain-of-function mutation BMC MEDICAL INFORMATICS AND DECISION MAKING
2015Context-based resolution of semantic conflicts in biological pathways BMC MEDICAL INFORMATICS AND DECISION MAKING
2015Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsyNATURE MEDICINE
2014A Systems Approach to Predict Oncometabolites via Context-Specific Genome-Scale Metabolic Networks PLOS GENETICS
2013Evaluating genome architecture of a complex region via generalized bipartite matching BMC BIOINFORMATICS
2013Wessim: a whole-exome sequencing simulator based on in silico exome captureBIOINFORMATICS
2013Reprever: resolving low-copy duplicated sequences using template driven assembly NUCLEIC ACIDS RESEARCH
2013Virmid: accurate detection of somatic mutations with sample impurity inference GENOME BIOLOGY
2012De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephalyNATURE GENETICS
2011Context-dependent transcriptional regulations between signal transduction pathways BMC BIOINFORMATICS
2011Exploring molecular links between lymph node invasion and cancer prognosis in human breast cancer BMC SYSTEMS BIOLOGY
2009Mining metastasis related genes by primary-secondary tumor comparisons from large-scale databases BMC BIOINFORMATICS
2008Computational identification of significantly regulated metabolic reactions by integration of data on enzyme activity and gene expression BMB REPORTS
2007BioCAD: an information fusion platform for bio-network inference and analysis BMC BIOINFORMATICS