| 15 | 박유미 | CNV calling using SNP array-based genotyping from UK Biobank | TopicSem |
| 18 | 유준기 | Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity | |
J.Club |
| 25 | 조민아 | Association analysis-Plink and Snpsift | SysBiol |
| 07 | 한봄 | Understanding HLA associations from SNP summary association statistics | |
J.Club |
| 20 | 한봄 | Cross-ethnicity tagging SNPs for HLA alleles associated with adverse drug reaction | |
J.Club |
| 07 | 박유미 | Finding indirect associations of tagging SNPs with MDD | TopicSem |
| 21 | 민병주 | Ampliseq based ADR(+ PGx SNP) targeted panel | TopicSem |
| 31 | 안세환 | Visualization portal for genetic variation(VizGVar): a tool for interactive visualization of SNPs and somatic mutations in exons, genes and protein domains | |
J.Club |
| 08 | 서명의 | Reinforcement for low coverage regions in DRP290 SNP Panel and LT Ampliseq WES | TopicSem |
| 04 | 서명의 | Experimental modification of Exome + DRP290 SNP Panel and 2nd test result | TopicSem |
| 01 | 서명의 | Design of Exome + DRP290 SNP Panel and experimental modification | TopicSem | |
| 02 | 박호경 | SSRIs drugs with Pharmacogenomic snp and adr | SysBiol |
| 16 | 박유미 | Finding indirect associations of tagging SNPs with variant angina | TopicSem |
| 01 | 김주연 | ADR risk determination according to FDA or PREDICT SNP genotype using synthetic association | TopicSem |
| 23 | 김주연 | Chromosomal distribution of variants synthetically associated with pharmacogenomic SNPs | SysBiol |
| 09 | 김주연 | Gene score distribution of genes including or proximate to pharmacogenomic SNPs | TopicSem |
| 20 | 서희원 | Comparison between the results of NGS and SNP Type Assays | TopicSem |
| 02 | 박유미 | HAPGEN2 : simulation of multiple disease SNPs | xMutant |
| 17 | 엄세인 | Trait-Associated SNPs Are More Likely to Be eQTLs. Annotation to Enhance Discovery from GWAS | |
J.Club |
| 09 | 서희원 | Systematic identification of relationship between marker SNP and cancer susceptibility gene | TopicSem |
| 11 | 임재현 | How SNP heterozygosity affects gene expressions | SysBiol |
| 04 | 이수연S | Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci | |
J.Club |
| 16 | 임영균 | SNPChase: correcting errors from diverse literatures and SNV databases | TopicSem | |
| 18 | 서희원 | Screening of association between marker SNPs and gene score | xMutant |
| 04 | 임영균 | SNPChase: correcting errors from diverse literatures and SNV databases | TopicSem |
| 10 | 임영균 | SNPChase: correcting errors from diverse literatures and SNV databases | TopicSem | |
| 12 | 임영균 | SNPChase: correcting errors from diverse SNV databases for SNVs | Seminar | |
| 31 | 임영균 | SNPChase: correcting errors from diverse literatures and SNV databases | TopicSem |
| 10 | 임영균 | SNPChase: correcting errors from diverse SNV databases for SNVs | TopicSem |
| 01 | 이수연S | SNP prioritization | TopicSem |
| 09 | 이수연S | SNPranker 2.0: a gene-centric data mining tool for diseases associated SNP prioritization in GWAS. | |
J.Club |
| 24 | 김지훈 | SNPedia: a wiki supporting personal genome annotation, interpretation and analysis | |
J.Club |
| 23 | 박찬희 | SNP and Indel Identification Variant Analysis and Annotation | |
TopicSem |
| 25 | 김도균 | SNP database | TopicSem |
| 02 | Rocky | [Replication] - Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes | xMutant |
| 10 | 서희원 | SNP Set Enrichment Analysis Associations with Rare Variants | SysBiol | |
| 10 | 김지훈 | Building SNP-Phenotype association database | |
SysBiol |
| 28 | 한현욱 | From SNPs to pathway | MAInfo |
| 11 | 서희원 | Gene-set wise approach for disease susceptibility using SNP profiles. | TopicSem | |
| 27 | 조용래 | Disease-associated SNP Database | SysBiol |
| 10 | Rocky | Computational prediction of target SNPs affecting miR-mRNA interaction | TopicSem |
| 20 | Rocky | Computational prediction of target SNPs affecting miR-mRNA interaction | TopicSem |
| 15 | Rocky | Investigating SNPs residing in the MicroRNA-Binding Sites: Method of study | TopicSem |
| 05 | Rocky | Investigating SNPs residing in the MicroRNA-Binding Sites � progress | TopicSem |
| 24 | Rocky | Investigating SNPs residing in the MicroRNA-Binding Sites from GWAS on Cancer Related Genes | Seminar |
| 19 | 송영수 | Lethal combinations of SNPs | MAInfo |
| 02 | 이수연S | Copy number variation databases and SNP DATABASE LIST | MAInfo |
| 29 | 김도균 | Xperanto-SNP: A web-based integrated management system for genetical genomics (Adding DACE module) | Seminar |
| 07 | 김도균 | Progress in Xperanto-SNP: Genotyping and detecting copy number modules embedded | Seminar |
| 19 | 김도균 | Identify co-effects of SNP and CNV on gene expression | Seminar |
| 09 | 김도균 | Xperanto-SNP draft | Seminar | |
| 14 | 김도균 | SNP@Promoter: a database of human SNPs (Single Nucleotide | |
J.Club |
| 23 | 김도균 | Integrated association studies for SNPs and CNVs with gene expression data | Seminar |
| 19 | 김도균 | SNP database test | Seminar |
| 14 | 김도균 | SNP array 5.0 analysis | Seminar | |
| 19 | 김도균 | SNPLims: a data management system for genome wide association studies | |
J.Club |
| 28 | 김도균 | SNP database Test | Seminar |
| 10 | 김도균 | ADRSNP system(약물이상반응 유전체연구) [약물유전체] | Seminar |
| 08 | 김도균 | A framework for integration of probe-level data from heterogeneous microarray platforms (SNP chip) | Seminar |
| 09 | 김도균 | Progress in Xperanto-SNP | Seminar |
| 23 | 김도균 | Progress in Xperanto-SNP | Seminar |
| 11 | 김도균 | CRLMM (Corrected Robust Linear Model with Maximum Likelihood Distance) [snp, genotyping] | Seminar |
| 06 | 김도균 | Work plan: Integrated SNP database and Analysis system [SNP, CNV, system] | Seminar | |
| 20 | 김도균 | Copy number and loss of heterozygosity estimation [CNV, SNP, LOH] | Seminar |
| 20 | 김도균 | Effects of copy number variations on classical genetic studies [SNP, CNV] | Seminar |
| 30 | 김도균 | Analysis plan for GAW data [CNV, Genome-wide association, SNP] | Seminar |
| 15 | 조성범 | SNP Chip analysis | Seminar | |
| 27 | 조성범 | Lung cancer genome analysis with SNP arrays | |
J.Club |
| 24 | 조성범 | SNP Chip Analysis | Seminar |
| 11 | 우정훈 | Extensive information for SNP chip analysis | xMutant |
| 04 | 박찬희 | Finding human SNPs miRNA genomic position related | xMutant | |
| 17 | 김민구 | FESD: a Functional Element SNPs Database in human | SysBiol |
| 21 | 김옥구 | 전자 증례기록지에서의 SNP 입력 설계 | BioEMR |
| 09 | 박찬희 | GRIP에서의 SNP data | MAInfo | |
| 25 | 박찬희 | Personalized and Automated dbSNP Surveillance System | |
J.Club |
| 23 | 박찬희 | SNPper: retrieval and analysis of human SNPs | |
J.Club |