Catholic Center for
Precision Medicine Research
Catholic Center for
Precision Medicine Research
Welcome to the Catholic Centre for Precision Medicine Research.
The Catholic Precision Medicine Research Center (PMRC) is dedicated to advancing translational medicine, bridging the gap between basic research and clinical practice. We lead patient-centered precision medicine research through artificial intelligence and state-of-the-art genomic analysis technologies.
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Our goal is to pioneer a new paradigm in precision medicine by leveraging AI technology and to realize data-driven personalized treatments.Ā
Developing and advancing precision medicine analysis technologiesĀ
Providing precision medicine education for medical professionals and researchersĀ Ā
Supporting genomic data production and AI-based analysisĀ
Creating innovative models through industry-academia collaborationĀ
š¬ Advanced Genomics Research Ā We are leading academic advancements in the precision medicine field by conducting national research projects and publishing papers in prestigious SCI-indexed international journals.Ā
š¤ AI-Based Precision Medicine Ā We utilize artificial intelligence and machine learning to analyze vast genomic data and develop predictive models for early disease detection.Ā
š Professional Education Programs Ā We offer hands-on training and workshops for medical professionals and researchers on topics such as genomic big data analysis and Next-Generation Sequencing (NGS).Ā
š Global Network Ā We are building a collaborative network with world-class researchers by co-hosting domestic and international academic conferences and organizing symposiums.Ā
š” Technology Development and Commercialization Ā We develop technologies such as rapid on-site infection tests and AI diagnostic algorithms, pursuing commercialization through patent applications to translate research outcomes into practical clinical applications.Ā
𧬠Genomic Analysis ServicesĀ
Cancer Gene Panel Analysis: Genetic mutation testing for personalized cancer treatment.Ā
Whole Exome Sequencing (WES): Analyzing all protein-coding genes to identify the causes of rare diseases.Ā
Whole Genome Sequencing (WGS): Decoding an individual's entire genetic makeup to provide comprehensive health information.Ā
Long-Read Sequencing: Precisely analyzing complex genetic variations that are difficult to detect with conventional methods.
Single-Cell Analysis: Investigating disease mechanisms by analyzing gene expression at the individual cell level.Ā
AI Data Analysis: Interpreting complex genomic data and deriving clinical insights using artificial intelligence.Ā
Location & Access
By Subway:
From Express Bus Terminal Station (Lines 3 & 7): Approximately a 200m walk from Exit 4.
From Seoul Nat'l Univ. of Education Station (Lines 2 & 3): Approximately a 1km walk from Exit 7.
By Shuttle Bus:
Express Bus Terminal Station (Lines 3, 7, 9): Board at the bus stop in front of Exit 3.
Seocho Station (Line 2): Board at the bus stop in front of Exit 7.
Address:Ā
#3017-2, Institute of Biomedical Industry, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul
Phone: +82-2-3147-9008