| 15 | 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 | Finding indirect associations of tagging SNPs with MDD | TopicSem |
| 21 | κ | 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 | Reinforcement for low coverage regions in DRP290 SNP Panel and LT Ampliseq WES | TopicSem |
| 04 | Experimental modification of Exome + DRP290 SNP Panel and 2nd test result | TopicSem |
| 01 | Design of Exome + DRP290 SNP Panel and experimental modification | TopicSem | ||
| 02 | ȣ | SSRIs drugs with Pharmacogenomic snp and adr | SysBiol |
| 16 | Finding indirect associations of tagging SNPs with variant angina | TopicSem |
| 01 | ֿ | ADR risk determination according to FDA or PREDICT SNP genotype using synthetic association | TopicSem |
| 23 | ֿ | Chromosomal distribution of variants synthetically associated with pharmacogenomic SNPs | SysBiol |
| 09 | ֿ | Gene score distribution of genes including or proximate to pharmacogenomic SNPs | TopicSem |
| 20 | Comparison between the results of NGS and SNP Type Assays | TopicSem |
| 02 | HAPGEN2 : simulation of multiple disease SNPs | xMutant |
| 17 | Trait-Associated SNPs Are More Likely to Be eQTLs. Annotation to Enhance Discovery from GWAS | |
J.Club |
| 09 | Systematic identification of relationship between marker SNP and cancer susceptibility gene | TopicSem |
| 11 | How SNP heterozygosity affects gene expressions | SysBiol |
| 04 | ̼S | Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci | |
J.Club |
| 16 | ӿ | SNPChase: correcting errors from diverse literatures and SNV databases | TopicSem | |
| 18 | Screening of association between marker SNPs and gene score | xMutant |
| 04 | ӿ | SNPChase: correcting errors from diverse literatures and SNV databases | TopicSem |
| 10 | ӿ | SNPChase: correcting errors from diverse literatures and SNV databases | TopicSem | |
| 12 | ӿ | SNPChase: correcting errors from diverse SNV databases for SNVs | Seminar | |
| 31 | ӿ | SNPChase: correcting errors from diverse literatures and SNV databases | TopicSem |
| 10 | ӿ | SNPChase: correcting errors from diverse SNV databases for SNVs | TopicSem |
| 01 | ̼S | SNP prioritization | TopicSem |
| 09 | ̼S | SNPranker 2.0: a gene-centric data mining tool for diseases associated SNP prioritization in GWAS. | |
J.Club |
| 24 | SNPedia: a wiki supporting personal genome annotation, interpretation and analysis | |
J.Club |
| 23 | SNP and Indel Identification Variant Analysis and Annotation | |
TopicSem | |
| 25 | 赵 | SNP database | TopicSem |
| 02 | Rocky | [Replication] - Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes | xMutant |
| 10 | SNP Set Enrichment Analysis Associations with Rare Variants | SysBiol | ||
| 10 | Building SNP-Phenotype association database | |
SysBiol | |
| 28 | From SNPs to pathway | MAInfo |
| 11 | Gene-set wise approach for disease susceptibility using SNP profiles. | TopicSem | ||
| 27 | 뷡 | 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 | ۿ | Lethal combinations of SNPs | MAInfo |
| 02 | ̼S | Copy number variation databases and SNP DATABASE LIST | MAInfo |
| 29 | 赵 | Xperanto-SNP: A web-based integrated management system for genetical genomics (Adding DACE module) | Seminar |
| 07 | 赵 | Progress in Xperanto-SNP: Genotyping and detecting copy number modules embedded | Seminar |
| 19 | 赵 | Identify co-effects of SNP and CNV on gene expression | Seminar |
| 09 | 赵 | Xperanto-SNP draft | Seminar | |
| 14 | 赵 | SNP@Promoter: a database of human SNPs (Single Nucleotide | |
J.Club |
| 23 | 赵 | Integrated association studies for SNPs and CNVs with gene expression data | Seminar |
| 19 | 赵 | SNP database test | Seminar |
| 14 | 赵 | SNP array 5.0 analysis | Seminar | |
| 19 | 赵 | SNPLims: a data management system for genome wide association studies | |
J.Club |
| 28 | 赵 | SNP database Test | Seminar |
| 10 | 赵 | ADRSNP system(̻ ü) [ü] | Seminar |
| 08 | 赵 | A framework for integration of probe-level data from heterogeneous microarray platforms (SNP chip) | Seminar |
| 09 | 赵 | Progress in Xperanto-SNP | Seminar |
| 23 | 赵 | Progress in Xperanto-SNP | Seminar |
| 11 | 赵 | CRLMM (Corrected Robust Linear Model with Maximum Likelihood Distance) [snp, genotyping] | Seminar |
| 06 | 赵 | Work plan: Integrated SNP database and Analysis system [SNP, CNV, system] | Seminar | |
| 20 | 赵 | Copy number and loss of heterozygosity estimation [CNV, SNP, LOH] | Seminar |
| 20 | 赵 | Effects of copy number variations on classical genetic studies [SNP, CNV] | Seminar |
| 30 | 赵 | Analysis plan for GAW data [CNV, Genome-wide association, SNP] | Seminar |
| 06 | SNP м Databasing [SNP, 500k, SNP CHIP] | Seminar | ||
| 08 | Modified Cluster index approach for storing SNP Chip Data | Seminar | ||
| 17 | 赵 | Progress in SNP analysis and databasing [SNP, 500k] | Seminar |
| 15 | SNP Chip analysis | Seminar | ||
| 27 | Lung cancer genome analysis with SNP arrays | |
J.Club |
| 24 | SNP Chip Analysis | Seminar |
| 11 | Extensive information for SNP chip analysis | xMutant |
| 04 | Finding human SNPs miRNA genomic position related | xMutant | ||
| 17 | α | FESD: a Functional Element SNPs Database in human | SysBiol |
| 21 | ʱ SNP Է | BioEMR |
| 09 | GRIP SNP data | MAInfo | ||
| 25 | Personalized and Automated dbSNP Surveillance System | |
J.Club |
| 23 | SNPper: retrieval and analysis of human SNPs | |
J.Club |