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 |