Lista de obras - Sangwoo Kim - Dominio Público Uruguay

A Therapeutic Strategy for Chemotherapy-Resistant Gastric Cancer via Destabilization of Both β-Catenin and RAS

scientific article published on 08 April 2019

A systems approach to predict oncometabolites via context-specific genome-scale metabolic networks

artículo científico publicado en 2014

AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing

artículo científico publicado en 2017

An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development

artículo científico publicado en 2015

An Improved, Assay Platform Agnostic, Absolute Single Sample Breast Cancer Subtype Classifier

scientific article published on 25 November 2020

Analysis of Whole Transcriptome Sequencing Data: Workflow and Software

artículo científico publicado en 2015

BAMixChecker: an automated checkup tool for matched sample pairs in NGS cohort

scientific article published on 01 November 2019

BioCAD: an information fusion platform for bio-network inference and analysis

artículo científico publicado en 2007

Brain somatic mutations in cause intractable epilepsy with aberrant N-glycosylation

article published in 2018

Brain somatic mutations observed in Alzheimer's disease associated with aging and dysregulation of tau phosphorylation

artículo científico publicado en 2019

CRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individual

scientific article published on 20 January 2020

Characteristic gene alterations in primary gastrointestinal T- and NK-cell lymphomas

artículo científico publicado en 2019

Context-based resolution of semantic conflicts in biological pathways

artículo científico publicado en 2015

Context-dependent transcriptional regulations between signal transduction pathways ⬇️

artículo científico publicado el 13 de enero de 2011

Cross-species oncogenic signatures of breast cancer in canine mammary tumors

artículo científico publicado en 2020

De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly

artículo científico publicado en 2012

Establishment of reference standards for multifaceted mosaic variant analysis

publication published on 03 February 2022

Evaluating genome architecture of a complex region via generalized bipartite matching

artículo científico publicado en 2013

Exome sequencing reveals recurrent REV3L mutations in cisplatin-resistant squamous cell carcinoma of head and neck

artículo científico publicado en 2016

Exploring molecular links between lymph node invasion and cancer prognosis in human breast cancer.

artículo científico publicado en 2011

Identification of genomic features in the classification of loss- and gain-of-function mutation.

artículo científico publicado en 2015

Impact of mouse contamination in genomic profiling of patient-derived models and best practice for robust analysis

artículo científico publicado en 2019

Isoform specific gene expression analysis of KRAS in the prognosis of lung adenocarcinoma patients.

artículo científico publicado en 2018

Mining metastasis related genes by primary-secondary tumor comparisons from large-scale databases

scientific article published on 19 March 2009

Pilot Study of a Next-Generation Sequencing-Based Targeted Anticancer Therapy in Refractory Solid Tumors at a Korean Institution

artículo científico publicado en 2016

Reprever: resolving low-copy duplicated sequences using template driven assembly

artículo científico publicado en 2013

Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia

artículo científico publicado en 2017

Somatic mutation driven codon transition bias in human cancer

artículo científico publicado en 2017

The use of technical replication for detection of low-level somatic mutations in next-generation sequencing

artículo científico publicado en 2019

Virmid: accurate detection of somatic mutations with sample impurity inference

artículo científico publicado en 2013

Wessim: a whole-exome sequencing simulator based on in silico exome capture

artículo científico publicado en 2013

Whole-exome and whole-transcriptome sequencing of canine mammary gland tumors

artículo científico publicado en 2019

Lista de obras de Sangwoo Kim

A Therapeutic Strategy for Chemotherapy-Resistant Gastric Cancer via Destabilization of Both β-Catenin and RAS

A systems approach to predict oncometabolites via context-specific genome-scale metabolic networks

AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing

An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development

An Improved, Assay Platform Agnostic, Absolute Single Sample Breast Cancer Subtype Classifier

Analysis of Whole Transcriptome Sequencing Data: Workflow and Software

BAMixChecker: an automated checkup tool for matched sample pairs in NGS cohort

BioCAD: an information fusion platform for bio-network inference and analysis

Brain somatic mutations in cause intractable epilepsy with aberrant N-glycosylation

Brain somatic mutations observed in Alzheimer's disease associated with aging and dysregulation of tau phosphorylation

CRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individual

Characteristic gene alterations in primary gastrointestinal T- and NK-cell lymphomas

Context-based resolution of semantic conflicts in biological pathways

Context-dependent transcriptional regulations between signal transduction pathways ⬇️

Cross-species oncogenic signatures of breast cancer in canine mammary tumors

De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly

Establishment of reference standards for multifaceted mosaic variant analysis

Evaluating genome architecture of a complex region via generalized bipartite matching

Exome sequencing reveals recurrent REV3L mutations in cisplatin-resistant squamous cell carcinoma of head and neck

Exploring molecular links between lymph node invasion and cancer prognosis in human breast cancer.

Identification of genomic features in the classification of loss- and gain-of-function mutation.

Impact of mouse contamination in genomic profiling of patient-derived models and best practice for robust analysis

Isoform specific gene expression analysis of KRAS in the prognosis of lung adenocarcinoma patients.

Mining metastasis related genes by primary-secondary tumor comparisons from large-scale databases

Pilot Study of a Next-Generation Sequencing-Based Targeted Anticancer Therapy in Refractory Solid Tumors at a Korean Institution

Reprever: resolving low-copy duplicated sequences using template driven assembly

Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia

Somatic mutation driven codon transition bias in human cancer

The use of technical replication for detection of low-level somatic mutations in next-generation sequencing

Virmid: accurate detection of somatic mutations with sample impurity inference

Wessim: a whole-exome sequencing simulator based on in silico exome capture

Whole-exome and whole-transcriptome sequencing of canine mammary gland tumors