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Genome-wide copy number alteration and VEGFA amplification of circulating cell-free DNA as a biomarker in advanced hepatocellular carcinoma patients treated with Sorafenib

BMC cancer, 2019-04, Vol.19 (1), p.292-292, Article 292

2019

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Integrative modeling of tumor genomes and epigenomes for enhanced cancer diagnosis by cell-free DNA

Nature communications, 2023-04, Vol.14 (1), p.2017-2017, Article 2017

2023

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Development and performance evaluation of an artificial intelligence algorithm using cell-free DNA fragment distance for non-invasive prenatal testing (aiD-NIPT)

Frontiers in genetics, 2022-11, Vol.13, p.999587-999587

2022

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Shallow Whole-Genome Sequencing of Cell-Free DNA (cfDNA) Detects Epithelial Ovarian Cancer and Predicts Patient Prognosis

Cancers, 2023-01, Vol.15 (2), p.530

2023

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Liquid biopsy using cfDNA to predict radiation therapy response in solid tumors

Radiation oncology journal , 2023, 41(1), , pp.32-39

2023

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Clinically significant maternal X chromosomal copy number variation detected by noninvasive prenatal test

The journal of obstetrics and gynaecology research, 2019-09, Vol.45 (9), p.1925-1928

2019

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Genomic mutation profiling using liquid biopsy in Korean patients with prostate cancer: Circulating tumor DNA mutation predicts the development of castration resistance

Investigative and Clinical Urology, 2021, 62(2), , pp.224-232

2021

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Genomic analysis of Korean patients with advanced prostate cancer by use of a comprehensive next-generation sequencing panel and low-coverage, whole-genome sequencing

Investigative and Clinical Urology, 2019, 60(4), , pp.227-234

2019

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Understanding Disease Susceptibility through Population Genomics

Genomics & Informatics, 2012, 10(4), , pp.234-238

2012

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Advanced deep-learning algorithm for multi-cancer detection using cf-WGS

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.e13560-e13560

2023

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Genome-wide copy number alteration (CNA) of circulating cell-free DNA (cfDNA) as a prognostic biomarker in esophageal squamous cell carcinoma (ESCC)

Journal of clinical oncology, 2019-05, Vol.37 (15_suppl), p.e15582-e15582

2019

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Sensitive detection of cancer using deep learning model of cfDNA genome-wide methylation data

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.e18789-e18789

2022

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Liquid biopsy using cfDNA to predict radiation therapy response in solid tumors

Radiation oncology journal, 2023-03, Vol.41 (1), p.32-39

2023

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Abstract 4600: Biomarker analysis in circulating cell-free DNA in patients treated with sorafenib for advanced hepatocellular carcinoma

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4600-4600

2018

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Genome-wide and size-based cell-free DNA indices as predictive biomarkers for locally advanced esophageal squamous cell carcinoma treated with preoperative or definitive chemoradiotherapy

Current problems in cancer, 2021-06, Vol.45 (3), p.100685-100685, Article 100685

2021

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Genetic heterogeneity and prognostic impact of recurrent ANK2 and TP53 mutations in mantle cell lymphoma: a multi-centre cohort study

Scientific reports, 2020-08, Vol.10 (1), p.13359-13359, Article 13359

2020

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Chromosomal Instability in Cell-free DNA as a Prognostic Biomarker of Metastatic Hormone-sensitive Prostate Cancer Treated with Androgen Deprivation Therapy

European urology focus, 2023-01, Vol.9 (1), p.89-95

2023

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Targeted next generation sequencing of circulating tumor DNA provides prognostic information for management in breast cancer patients

Annals of translational medicine, 2022-01, Vol.10 (2), p.28-28

2022

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Abstract P4-12-12: Next generation sequencing-based analysis of BRCA1 and BRCA2 genes: Applicability for fast diagnostics of large samples

Cancer research (Chicago, Ill.), 2015-05, Vol.75 (9_Supplement), p.P4-P4-12-12

2015

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Abstract 6371: Deep learning algorithm for multi-cancer detection and classification using cf-WGS

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.6371-6371

2022

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Identification of a Novel De Novo Variant in the PAX3 Gene in Waardenburg Syndrome by Diagnostic Exome Sequencing: The First Molecular Diagnosis in Korea

Annals of Laboratory Medicine, 2015, 35(3), , pp.362-365

2015

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Understanding Disease Susceptibility through Population Genomics

Genomics & informatics, 2012, Vol.10 (4), p.234-238

2012

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Clinically significant maternal X chromosomal copy number variation detected by noninvasive prenatal test

The journal of obstetrics and gynaecology research, 2019, Vol.45 (9), p.1925-1928

2019

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Multi-domain modeling of Electric Power Steering with PMSM Drive System

2007 IEEE International Electric Machines & Drives Conference, 2007, Vol.2, p.1355-1360

2007

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Genome-wide copy number alteration and VEGFA amplification of circulating cell-free DNA as a biomarker in advanced hepatocellular carcinoma patients treated with Sorafenib

Integrative modeling of tumor genomes and epigenomes for enhanced cancer diagnosis by cell-free DNA

Development and performance evaluation of an artificial intelligence algorithm using cell-free DNA fragment distance for non-invasive prenatal testing (aiD-NIPT)

Shallow Whole-Genome Sequencing of Cell-Free DNA (cfDNA) Detects Epithelial Ovarian Cancer and Predicts Patient Prognosis

Liquid biopsy using cfDNA to predict radiation therapy response in solid tumors

Clinically significant maternal X chromosomal copy number variation detected by noninvasive prenatal test

Genomic mutation profiling using liquid biopsy in Korean patients with prostate cancer: Circulating tumor DNA mutation predicts the development of castration resistance

Genomic analysis of Korean patients with advanced prostate cancer by use of a comprehensive next-generation sequencing panel and low-coverage, whole-genome sequencing

Understanding Disease Susceptibility through Population Genomics

Advanced deep-learning algorithm for multi-cancer detection using cf-WGS

Genome-wide copy number alteration (CNA) of circulating cell-free DNA (cfDNA) as a prognostic biomarker in esophageal squamous cell carcinoma (ESCC)

Sensitive detection of cancer using deep learning model of cfDNA genome-wide methylation data

Liquid biopsy using cfDNA to predict radiation therapy response in solid tumors

Abstract 4600: Biomarker analysis in circulating cell-free DNA in patients treated with sorafenib for advanced hepatocellular carcinoma

Genome-wide and size-based cell-free DNA indices as predictive biomarkers for locally advanced esophageal squamous cell carcinoma treated with preoperative or definitive chemoradiotherapy

Genetic heterogeneity and prognostic impact of recurrent ANK2 and TP53 mutations in mantle cell lymphoma: a multi-centre cohort study

Chromosomal Instability in Cell-free DNA as a Prognostic Biomarker of Metastatic Hormone-sensitive Prostate Cancer Treated with Androgen Deprivation Therapy

Targeted next generation sequencing of circulating tumor DNA provides prognostic information for management in breast cancer patients

Abstract P4-12-12: Next generation sequencing-based analysis of BRCA1 and BRCA2 genes: Applicability for fast diagnostics of large samples

Abstract 6371: Deep learning algorithm for multi-cancer detection and classification using cf-WGS

Identification of a Novel De Novo Variant in the PAX3 Gene in Waardenburg Syndrome by Diagnostic Exome Sequencing: The First Molecular Diagnosis in Korea

Understanding Disease Susceptibility through Population Genomics

Clinically significant maternal X chromosomal copy number variation detected by noninvasive prenatal test

Multi-domain modeling of Electric Power Steering with PMSM Drive System

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