about
Analysis of Whole Transcriptome Sequencing Data: Workflow and SoftwareSomatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly.BioCAD: an information fusion platform for bio-network inference and analysis.Virmid: accurate detection of somatic mutations with sample impurity inferenceExploring molecular links between lymph node invasion and cancer prognosis in human breast cancer.Evaluating genome architecture of a complex region via generalized bipartite matchingA systems approach to predict oncometabolites via context-specific genome-scale metabolic networksIdentification of genomic features in the classification of loss- and gain-of-function mutation.Context-based resolution of semantic conflicts in biological pathwaysPilot Study of a Next-Generation Sequencing-Based Targeted Anticancer Therapy in Refractory Solid Tumors at a Korean InstitutionExome sequencing reveals recurrent REV3L mutations in cisplatin-resistant squamous cell carcinoma of head and neck.Wessim: a whole-exome sequencing simulator based on in silico exome capture.Reprever: resolving low-copy duplicated sequences using template driven assembly.An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical developmentMining metastasis related genes by primary-secondary tumor comparisons from large-scale databases.Somatic mutation driven codon transition bias in human cancer.AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing.Brain somatic mutations in cause intractable epilepsy with aberrant N-glycosylationThe use of technical replication for detection of low-level somatic mutations in next-generation sequencingIsoform specific gene expression analysis of KRAS in the prognosis of lung adenocarcinoma patients.Characteristic gene alterations in primary gastrointestinal T- and NK-cell lymphomasImpact of mouse contamination in genomic profiling of patient-derived models and best practice for robust analysisBrain somatic mutations observed in Alzheimer's disease associated with aging and dysregulation of tau phosphorylationWhole-exome and whole-transcriptome sequencing of canine mammary gland tumorsBAMixChecker: an automated checkup tool for matched sample pairs in NGS cohortCRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individualA Therapeutic Strategy for Chemotherapy-Resistant Gastric Cancer via Destabilization of Both β-Catenin and RAS
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Sangwoo Kim
@ast
Sangwoo Kim
@en
Sangwoo Kim
@es
Sangwoo Kim
@sl
type
label
Sangwoo Kim
@ast
Sangwoo Kim
@en
Sangwoo Kim
@es
Sangwoo Kim
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prefLabel
Sangwoo Kim
@ast
Sangwoo Kim
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Sangwoo Kim
@es
Sangwoo Kim
@sl
P106
P31
P496
0000-0001-5356-0827