09 | 윤미선 | Hierarchical RAG Enhances a Pharmacogenomic AI assistant in Guideline related Queries | TopicSem |
31 | 임성수 | LORIS robustly predicts patient outcomes with immune checkpoint blockade therapy using common clinical, pathologic and genomic features | ![]() |
J.Club |
17 | 윤미선 | Replication: Empowering personalized pharmacogenomics with generative AI solutions | TopicSem | |
22 | 차재현 | Proteogenomic characterization of pancreatic ductal adenocarcinoma | ![]() |
J.Club |
23 | 윤미선 | Replication: Empowering personalized pharmacogenomics with generative AI solutions | TopicSem |
29 | 윤미선 | Artificial intelligence-based translation and interpretation of pharmacogenomic analysis using Large Language Model | TopicSem |
24 | 유준기 | cLD Rare variant linkage disequilibrium between genomic regions identifies novel genomic interactions | ![]() |
J.Club |
28 | 유준기 | CoxPH model for cross-sectional genomic data | MAInfo |
15 | 이시은 | G-CDM : genomic information to current OMOP-CDM | SysBiol |
23 | 안세환 | Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank | ![]() |
J.Club |
18 | 윤미선 | Nine-gene pharmacogenomics profile service | MAInfo | |
18 | 윤미선 | Nine-gene pharmacogenomics profile service | MAInfo |
18 | 권호식 | Candidate genomic variations in patients with adverse reactions to contrast media | TopicSem |
22 | 윤미선 | The pharmacogenomic landscape of an Indigenous Australian population | ![]() |
J.Club |
31 | 차재현 | Genomic study of Major Depressive Disorder | TopicSem |
07 | 유준기 | Computational genomic approaches to interpret non-coding disease risk variants | MAInfo |
11 | 전예진 | GWAS in complex disease and pharmacogenomics | TopicSem | |
13 | 안세환 | A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants | ![]() |
J.Club |
20 | 권호식 | Potential genomic variations related with adverse effects of contrast media | TopicSem |
18 | 안세환 | Identification and functional validation of novel pharmacogenomic variants using a next-generation sequencing-based approach for clinical pharmacogenomics | ![]() |
J.Club |
12 | 안선주 | Pharmacogenomics Watch(PGWatch) - Intro, Terms, DB | TopicSem | |
30 | 윤미선 | Pharmacogenomic Profile of Korean population using whole genome sequencing (HLA) | TopicSem |
03 | 부은경 | An integral genomic signature approach for tailored cancer therapy using genome-wide sequencing data | ![]() |
J.Club |
26 | 윤미선 | Pharmacogenomic Profile of Korean population using WGS | TopicSem |
19 | 안세환 | PharmaKU: A web-based tool aimed at improving outreach and clinical utility of pharmacogenomics | ![]() |
J.Club |
22 | 윤미선 | Pharmacogenomic Profile of Korean population using whole genome sequencing_2 | TopicSem | |
26 | 전예진 | type of pharmacogenomic evidence and limitation | SysBiol |
23 | 안세환 | Dating genomic variants and shared ancestry in population scale sequencing data | ![]() |
J.Club |
04 | 배소정 | Loss of Bacitracin Resistance Due to a Large Genomic Deletion among Bacillus anthracis Strains | ![]() |
J.Club |
11 | 조민아 | Genozip: a universal extensible genomic data compressor | SysBiol | |
24 | 인턴 | Pharmacogenomics and individualized therapy through VCF analysis | ![]() |
TopicSem |
20 | ̿ | Allele-specific genomic data elucidate the role of somatic gain and copy-number neutral loss of heterozygosity in cancer | ![]() |
J.Club |
30 | 조동영 | Improving Genomic Discovery with Machine Learning Based Phenotyping | TopicSem |
10 | 홍진희 | Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood | ![]() |
J.Club |
03 | ֿ | Genomic variant analysis and interpretation for Parkinsons disease | TopicSem | |
03 | ֿ | Genomic variant analysis and interpretation for Parkinsons disease | TopicSem |
20 | 조원일 | Review: pharmacogenomics_lancet | SysBiol | |
26 | 유경훈 | ATAV - a comprehensive platform for population-scale genomic analyses | xMutant |
25 | 유경훈 | Comprehensive analysis to discover the genomic background of antidepressant drug response | TopicSem |
02 | Genomic sequencing for newborn screening: results of the NC NEXUS project | ![]() |
J.Club |
12 | 조민아 | Imaging genomics discovery of a new risk variant for Alzheimer | ![]() |
J.Club |
28 | ֿ | Population structure and pharmacogenomic risk stratification in the United States | ![]() |
J.Club |
26 | ֿ | Examining the impact of pharmacogenomics testing with UK Biobank and its use for ADR risk comparisons | TopicSem |
05 | 김지헌 | SWEDEGENE—a Swedish nation-wide DNA sample collection for pharmacogenomic studies of serious adverse drug reactions | ![]() ![]() |
J.Club |
31 | ֿ | Identifying populations likely to benefit from pharmacogenomic testing | SysBiol | |
31 | ֿ | Implementation of pharmacogenomics via a research biobank | BioEMR |
27 | ӿ | Identification of genomic markers affecting sentivity of tacrolimus | TopicSem |
18 | ֿ | Economic burden of adverse drug reactions and potential for pharmacogenomic testing in Singaporean adults | ![]() |
J.Club |
14 | ȿ | Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network | ![]() |
J.Club |
02 | 권호식 | MTX Genomic markers from literatures | xMutant | |
11 | ȿ | Pharmacogenomic clinical decision support design and multi-site process outcomes analysis in the eMERGE Network | ![]() |
J.Club |
09 | ̿ | Re-identification of individuals in genomic data-sharing beacons via allele inference | ![]() |
J.Club |
23 | 안세환 | GenIO: a phenotype-genotype analysis web server for clinical genomics of rare diseases | ![]() |
J.Club |
19 | 한봄 | Functional annotation of genomic variants in studies of late-onset Alzheimer | ![]() |
J.Club |
01 | 권호식 | The landscape of genomic alterations across childhood cancers | ![]() |
J.Club |
08 | Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines | ![]() |
J.Club |
26 | Radiogenomics for TNBC: Relationship between Microarray profile and radiomics texture data | xMutant |
17 | GA4GH and Google genomics | BioEMR | ||
26 | ֿ | Patient-Centered Precision Health In A Learning Health Care System: Geisingers Genomic Medicine Experience | ![]() |
J.Club |
21 | ӿ | Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics | ![]() |
J.Club |
17 | 정문경 | Genomic Landscape of Cell-Free DNA in Patients with Colorectal Cancer | ![]() ![]() |
J.Club |
06 | Pharmacogenomics of GPCR Drug Targets | ![]() |
J.Club | |
23 | KCDM genome and FHIR genomics | BioEMR |
02 | ȣ | SSRIs drugs with Pharmacogenomic snp and adr | SysBiol |
14 | ֿ | Multidisciplinary model to implement pharmacogenomics at the point of care | ![]() |
J.Club |
09 | ӿ | Integrative clinical genomics of metastatic cancer | ![]() |
J.Club |
25 | ȣ | SNRIs Antidepressants and Pharmacogenomic information | SysBiol | |
25 | ȣ | SNRIs Antidepressants and Pharmacogenomic information | SysBiol |
27 | ֿ | Creating a scalable clinical pharmacogenomics service with automated interpretation and medical record result integration-experience from a pediatric tertiary care facility | ![]() |
J.Club |
08 | MEREDITH:Clustering and Visualization tools for TCGA PAN-CANCER with multiplatform genomic data | MAInfo | ||
20 | ̰ȭ | Review Cases of Genomic Data Warehouse | SysBiol |
23 | ֿ | Chromosomal distribution of variants synthetically associated with pharmacogenomic SNPs | SysBiol | |
25 | Intern | (Replication) Genomic and Epigenomic Landscapes of Adult De Novo AML | ![]() |
Seminar |
05 | Integrative analysis for identifying the best anticancer therapy based on genomic features | SysBiol | ||
24 | The global spectrum of protein-coding pharmacogenomic diversity | ![]() |
J.Club |
17 | ȣ | Bina - develops next-generation genomic management | SysBiol |
19 | The human diseases network using genomic information | TopicSem | ||
21 | [REVIEW] Mutations and Drugs Portal(MDP) : A database linking drug response data and genomic information | xMutant |
18 | Research for investigating genomic characteristics in human disease network | TopicSem |
14 | ̰ȭ | Review:Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data | MAInfo |
19 | Proposal on Machine Learning Application to Cancer Pharmacogenomics | TopicSem |
09 | Interest in Study of Genomics of Drug Sensitivity in Cancer | TopicSem | ||
12 | ֿ | Electronic health record design and implementation for pharmacogenomics: a local perspective | ![]() |
J.Club |
27 | Research on Diabetes and Pharmacogenomics | TopicSem |
12 | ̰ȭ | Review: Personalized Pharmacogenomics: Predicting Efficacy and Adverse Drug Reactions | MAInfo | |
20 | κ | Cancer genomics: one cell at a time | ![]() |
J.Club |
16 | ̼S | Personal pharmacogenomics : pharmacological approach based on genomic variant | TopicSem |
13 | ֿ | Development and use of active clinical decision support for preemptive pharmacogenomics | ![]() |
J.Club |
01 | Personalized pharmacogenomics profiling using whole-genome sequencing | ![]() |
J.Club | |
22 | Interpretation of Genomic Variants Using a Unified Biological Network Approach | ![]() |
J.Club |
10 | ֿ | Review of FDA-approved drugs with pharmacogenomic information in their labeling | SysBiol | |
14 | Heritability and genomics of gene expression in peripheral blood | J.Club |
04 | Apply CCLE data to personal pharmacogenomics research | SysBiol | ||
10 | ̼S | Pharmsafe algorithm accuracy boosting using genomic feature and biological knowledge | TopicSem |
03 | ̼S | review of Pharmacogenomics(Pharmacogenomics in Action) | SysBiol | |
07 | ӿ | Integrative annotation of variants from 1092 humans: application to cancer genomics. | ![]() |
J.Club |
07 | ȼ | Clinical Cancer Genomics | TopicSem |
30 | Genomic Perturbation Network | TopicSem |
24 | The Exomes of the NCI-60 Panel: A Genomic Resource for Cancer Biology and Systems Pharmacology | ![]() |
J.Club |
01 | integrated genomic characterization of endometrial carcinoma | J.Club | ||
05 | ̼S | Personal phenotype ranking algorithm based on genomic variation& | TopicSem |
15 | Medappllo : Drug ranking forecast algorithm based on personal genomic variation | TopicSem | ||
17 | ̼S | PRAGEN : personal Phenotype Ranking Algorithm based on GENomic variation | TopicSem |
16 | Genomic Variation landscape of the human gut microbiome | ![]() |
J.Club |
24 | 赵 | Graph- and kernel-based integrative analyses of multi-layers of heterogeneous genomic data ( ϻ) | TopicSem |
14 | Aplication of pharmacogenomic knowledge to clinic | SysBiol |
16 | 赵 | Graph-based integration with heterogeneous genomic data and genomic knowledge | TopicSem |
25 | Rocky | The global impact of genomic variations on miRNAs and their regulatory genes using whole genome sequencing data in human cancer | Seminar | |
25 | 赵 | Graph based integration with genomic data and genomic knowledge | Seminar | |
25 | Prioritization of adverse drug reaction susceptibility based on personal genomic variants | Seminar |
14 | Summary of pharmacogenomic research | SysBiol | ||
19 | Hapmap data processing for analysis in pharmacogenomics | TopicSem |
02 | Contribution of Genomic Variants to Human Phenotypes in Functional Genomics | TopicSem | ||
09 | ۿ | Development of Measurement of Genomic Similarity between Human Individuals | TopicSem |
16 | ۿ | B & T Cell Metagenomics and Clinical Applications | TopicSem | |
21 | 赵 | Plan for integration with inter-relationship between sample features belonging to different layers of genomic data | TopicSem |
26 | ̼ | miRNA-mRNA pairing relationship ? genomic locations and co-transcriptomics data set | TopicSem |
15 | Interpretation of high-throughput genomic data using integrated biological pathway resources and biomedical knowledge | TopicSem |
02 | ̼S | ArrArrayExpress update from an archive of functional genomics experiments to the atlas of gene expression | ![]() |
J.Club |
01 | 赵 | IntOGen: integration and data mining of multidimensional oncogenomic data | ![]() |
J.Club |
31 | ۿ | Annotation of Individual Human Genomic DNAs | Seminar |
09 | ̼S | NCBI GEO: archive for high-throughputfunctional genomic data | ![]() |
xMutant |
16 | 赵 | A statistical framework for genomic data fusion | ![]() |
J.Club |
30 | 赵 | A graph-based integration of multidimensional cancer genomics data | Seminar |
02 | 赵 | Integration of multidimensional genomic data (Databasing TCGA data) | Seminar | |
21 | Genomic signatures to guide the use of chemotherapeutics | ![]() |
J.Club |
03 | Genomic coordinate overlapping similarity in mutually llinked set | Seminar | ||
26 | 赵 | Pharmacogenomics 2009 Review | J.Club |
22 | 赵 | Instrumenting the health care enterprise for discovery research in the genomic era | ![]() |
J.Club |
16 | 赵 | Developing a database for integrative genomics (application in genetical genomics) | Seminar |
07 | 赵 | GenomeGraphs: integrated genomic data visualization with R | ![]() |
J.Club |
07 | 赵 | SIGMA2: A system for the integrative genomic multi-dimensilnal analysis of cancer genomes, epigenomes, and transcriptomes | ![]() |
J.Club |
22 | 赵 | MD-SeeGH: a platform for integrative analysis of multi-dimensional genomic data | ![]() |
J.Club |
25 | Integrative Genomic Analysis | J.Club |
28 | CelMAP: genomic and mRNA sequence | Seminar |
05 | A semantic grid infrastructure enabling integrated access and analysis of multilevel biomedical data in support of postgenomic clinical trials on cancer. | ![]() |
J.Club |
28 | ̼ | Genomic and epigenetic alterations deregulate microRNA expression in human epithelial ovarian cancer | ![]() |
J.Club |
17 | 赵 | The pharmacogenetics and pharmacogenomics knowledge base: accentuating the knowledge | ![]() |
J.Club |
25 | 赵 | Progress in Pharmacogenomics project [ü] | Seminar |
08 | Genomic analysis of human microRNA transcripts | ![]() ![]() |
J.Club | |
14 | Comparison of genomic structure between intronic and intergenic miRNAs | Seminar |
06 | Identifying Genomic Regulators of Set-Wise Co-Expression (presentation for BIBE 2007 ) | J.Club |
14 | A genomic code for nucleosome positioning | ![]() |
J.Club | |
21 | Evidence of spatially bound gene regulation in Mus musculus: decreased gene expression proximal to microRNA genomic location | ![]() ![]() |
J.Club |
13 | Complex trait analysis using set-wise genetical genomics approach ( ǥ final) | Seminar | ||
16 | Finding function: evaluation methods for functional genomic data. | ![]() ![]() |
J.Club |
28 | Normalization procedures and detection of linkage signal in genetical-genomics experiments. | ![]() ![]() |
J.Club |
25 | Inferring Causal Association among Pathways (ICAP)by Genetical Genomics approach | Seminar |
03 | The graPT: Genomic inteRpreter About Predictive Toxicology | ![]() |
Seminar |
09 | An integrative genomics approach to infer causal associations between gene expression and disease [genetical genomics] | ![]() ![]() |
J.Club |
14 | Analysis plan for "Genetic Analysis Workshop" data. [genetical genomics] | MAInfo |
07 | Research plan (about toxicogenomics meta DB) | BioEMR |
09 | Xperanto-Tox: strategy for data modeling toxicogenomics experiment | BioEMR |
01 | Xperanto-Tox: Integration of Xperanto and Xperanto-TMA for toxicogenomics | BioEMR | ||
05 | Comparative Genomics for Orientia | Seminar |
15 | A Framework for storing various biological material information and functional genomics data (Feasibility Study) | BioEMR |
11 | Standardization initiatives in the (eco)toxicogenomics domain: a review | ![]() ![]() |
J.Club |
30 | Genomic Messaging System and DNA Mark-Up Language for Information-Based Personalized Medicine with Clinical and Proteome Research Applications | ![]() ![]() |
J.Club |
04 | Finding human SNPs miRNA genomic position related | xMutant | ||
31 | Cancer Genomics Object Model | BioEMR |
26 | Implementation of Cancer Genomics Object Model [ClinInfo] | Seminar |
17 | ¼ | GenRate: A Generative Model That Finds and Scores New Genes and Exons in Genomic Microarray Data [PSB] | ![]() |
J.Club |
18 | Cancer Genomics Object Model(2) | BioEMR |
27 | ѹ̷ | Detection of low level genomic alterations by comparative genomic hybridization based on cDNA micro-arrays | ![]() ![]() |
J.Club |
29 | PharmacoGenomics ɺо Ȳ | xMutant |
28 | An object model and database for functional genomics. | ![]() ![]() |
J.Club |
10 | How (not) to protect genomic data privacy in a distributed network: using trail re-identification to evaluate and design anonymity protection systems. | ![]() ![]() |
J.Club |
05 | ArrayTrack.Supporting Toxicogenomic Research at the U.S. Food and Drug Administration National Center for Toxicological Research | ![]() ![]() |
J.Club |
15 | GoMiner: a resource for biological interpretation of genomic and proteomic data | ![]() ![]() |
J.Club |
04 | α | Comparing protein abundance and mRNA expression levels on a genomic scale | ![]() ![]() |
J.Club |
27 | (H) | Visualizing Genomic Data Microarrays | Seminar |
09 | XML documentation of biopathways and their simulations in Genomic Object Net | ![]() ![]() |
J.Club |
23 | Prediction of probable genes by Fourier analysis of genomic sequences | ![]() ![]() |
J.Club |
28 | Identification of Genes in Human Genomic DNA | Seminar |