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BioProject ID : KAP220183

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Project title : Data Center for Genomic Medicine

Summary 내용시작

Submitter

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Name Kim Hyung Lae
Organization Ewha University-Industry Collaboration Foundation
Department Department of Biochemistry

Date

Date

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Registration Date 2022-04-12

Project Design

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NTIS Number -
Project Title Data Center for Genomic Medicine
Relevance medical
Description "○ Support for integration and analysis of genomic data such as NGS produced in the multi-ministerial genome project Standardization of raw data, primary and secondary processing, and integrated genome resource DB are established by targeting genome resources that can be open and shared cooperative research for detailed tasks of the genome business. ○ Support for high-performance computer-based cooperative research Platform and analysis service (genome farm) operation for advanced utilization of integrated resources Establishment of cooperative system through integrated genomic resource and human resource consortium ○ Education to strengthen the capabilities of human genome analysis researchers in customized medical care (training using high-performance computers, etc.) ○ International cooperation research in cloud environment Participation in clinical genome research based on international cooperation to verify platform effectiveness (pan-caner project) Supports international level convergence research by producing and analyzing data necessary for disease genome research ○ Expand support for disease genomic research Derivation of analysis results for phase estimation and recombination through WGS analysis of 3 or more extended households Support for HPC-based meta-research and support for confirmation and expansion of disease genomic research"
Project Data Type * Transcriptome or Gene Expression
Sample Scope * Multiisolate

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Relations 내용시작

Sample Group

BioSample
Accession ID
Project Title
Sample Type
Registration Date
KASG220280 Discovery of cancer-related candidate genes by analyzing genomic mutations in intractable lung cancer disease Human sample 2022-04-12
KASG220295 Identification of genetic variants in obesity Human sample 2022-04-12
KASG220281 Blood cancer (AML) whole genome sequencing Human sample 2022-04-12
KASG220287 Gut metagenome study of Parkinson disease Human sample 2022-04-12
KASG220257 Path to the obese phenotype through the interaction of personality genome, brain region(MRI), behavior-diet and gut microbiome Human sample 2022-04-12
KASG220284 A study on the discovery of genes affecting the onset and clinical phenotype of chronic obstructive pulmonary disease in Koreans through genotype analysis Human sample 2022-04-12
KASG220265 Whole genome sequencing on blood cancer Human sample 2022-04-12
KASG220294 Identification of Genetic Variants in Parkinson disease Human sample 2022-04-12
KASG220289 Whole genome-sequencing for multiple myeloma Human sample 2022-04-12
KASG220249 Trio Phasing Study Human sample 2022-04-12
KASG220268 Whole genome sequencing on lung cancer Human sample 2022-04-12
KASG220263 Identification of genetic variants associated with health screening examination phenotypes, behavioral and personality traits by genomic collaboration under the HPC platform Human sample 2022-04-12
KASG220262 Characterization of blood metagenome by 16S amplicon sequencing Human sample 2022-04-12
KASG220285 Characterization of blood metagenome by 16S amplicon sequencing Human sample 2022-04-12
KASG220250 Blood Cancer Genetic Variation Analysis Human sample 2022-04-12
KASG220245 Whole genome sequencing of lung cancer Human sample 2022-04-12
KASG220270 Characterization of blood metagenome by 16S amplicon sequencing Human sample 2022-04-12
KASG220261 Discovery of specific genetic changes in wild type EGFR lung adenocarcinoma patients Human sample 2022-04-12
KASG220264 Discovering new disease progression factors through genomic analysis related to disease progression in patients with intractable malignant blood disease Human sample 2022-04-12
KASG220273 Acute myeloid leukemia customized medical clinical translational study Human sample 2022-04-12
KASG220277 Identification of the genetic cause, molecular diagnosis, and customized treatment method through the establishment of large-scale whole exome data of Charcot-Marie-Tooth disease Human sample 2022-04-12

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