ScholarWorks@Soongsil University: Kim, Sangsoo

Detailed Information

Kim, Sangsoo (김상수)

College of Natural Sciences (Department of Bioinformatics & Life Science)

Research Area: 생명정보학, 유전체정보학, bioinformatics, genome informatics

Tel
Homepage

ResearcherID ORCiD Scopus Google Scholar ID ResearchGate

Keyword

genomewide association study:5||SNP:4||s disease:3||GWAS:3||Korea:2||genetic variation:2||QTL mapping:2||machine learning:2||Deep learning:2||HapMap:2||RNA sequencing:2||Colorectal neoplasms:2||Crohn&apos:2||NGS:2||Bioinformatics:2||bioinformatics:2||deep learning:2||Mass screening:2||personal genomics:2||phasing:2||phylogeny:2||single nucleotide polymorphism:2||Cluster calculations:1||Coexpression network:1||Combinatorial histone modifications:1||Comparative genomics:1||Computational biology:1||Crohn&:1||Cryptosporidium parvum:1||Crystal structure:1||Crystal twinning:1||CysQ:1||Cytosine:1||DNA Methylation:1||DNA methylation:1||DNA transfering:1||Data mining:1||De novo assembly:1||Differential modifications:1||EED:1||Entropy:1||Essential genes:1||Evolutionary adaptation:1||Ezh2:1||Felidae:1||Gene Ontology:1||Gene ontology:1||Geneset analysis:1||Genetic algorithms:1||Genetic risk score:1||Genome Browser:1||Genome sequences:1||Genomewide association study:1||Gold atom cluster calculation:1||Gold nanoparticles:1||H3K27me3:1||Hepatitis B virus X (HBx)transgenic mice:1||Hepatocellular carcinoma:1||Indexes:1||KARE:1||Korea Patented Biological Sequences:1||Korean patent sequences:1||Leopard:1||Ligandinduced conformational change:1||Machine learning:1||Mendelian inconsistency:1||Microbiome:1||Microorganisms:1||N6,N6Dimethyladenine:1||N6Methyladenine:1||NFIA:1||Naive CD4+T cells:1||Neural networks:1||Notch pathway:1||Optic disc swelling:1||Optic neuropathy:1||PLINK:1||PRC2:1||Partial AUC:1||Patome@Korea:1||Prediction:1||Pseudo symmetry:1||Pseudopapilledema:1||Psoriasis:1||Quantitative genetics:1||RNA secondary structure:1||RNASeq:1||RNAseq:1||Raman ringbreathing mode:1||Raman spectroscopy:1||RefSeq:1||Regulatory network:1||Repeat element:1||Risk assessment:1||SNP imputation:1||SQTLs:1||Sequential analysis:1||Shiny:1||Singlecell RNA sequencing:1||Speed of sound:1||Systematics:1||Tautomer:1||Tautomers:1||Taxonomy:1||Transcription factor:1||Unet:1||Wnt pathway:1||advanced colorectal neoplasia:1||and BiofunctionPatent Association Maps:1||antiTNF:1||antibodymediated rejection:1||association rule mining:1||astrocyte:1||blood pressure:1||cisacting:1||coexpression network:1||colorectal cancer:1||colorectal cancer screening:1||comparative:1||conserved domain:1||copy number variation (CNV):1||core search:1||coupon collection problem:1||data consistency:1||data mining:1||database:1||disease susceptibility:1||disease:1||docker:1||erythrocyte:1||ethnic difference:1||ethnic group:1||expressed sequence tag frequency:1||expression profiling:1||expression quantitative trait loci:1||frizzled related protein1:1||gastric cancer:1||gene set:1||gene set analysis:1||gene synteny:1||gene:1||genepatent map:1||genetic features:1||genome browser:1||genome rearrangement:1||genomewide association:1||genotype:1||genotypingbysequencing:1||global BPgen:1||haplotype:1||haplotypes:1||haploview:1||hematocrit:1||hemoglobin:1||hepatocellular carcinoma:1||horizontal gene transfer:1||inflammatory bowel disease:1||kidney transplantation:1||low density lipoprotein cholesterol:1||magnetic resonance imaging:1||mammalian genomes:1||medaka fish:1||meningioma:1||metaanalysis:1||metamicrobial feature:1||metaanalysis:1||miassembly:1||microarray:1||microbial community analysis:1||microbial module:1||microbial network analysis:1||microbiome modeling:1||minimum SNP:1||mitochondrial DLoop:1||msDNA:1||multiallelic CNV genotype:1||multivariate phenotypes:1||myelination:1||neighbourjoining:1||network:1||nextgeneration sequencing:1||nuclear mitochondrial DNA:1||numt:1||oligodendrocyte:1||pathway:1||pattern discovery:1||pericentric:1||pharmacogenomics:1||phylogenetic tree:1||phylogeography:1||plant mitochondrial DNA:1||pleiotropy:1||postGWAS:1||prediction:1||prognosis:1||quantitative traits:1||random superset selection:1||recombination:1||red blood cell:1||reference genome:1||regulation:1||regulator:1||repeat map:1||replication:1||retron:1||reverse transcriptase:1||sQTLs:1||semantic similarity:1||sequence motif:1||singlenucleotide polymorphism:1||singlenucleotide polymorphism (SNP):1||subarachnoid aneurismal hemorrhage (SAH):1||subtelomeric:1||sulfur assimilation:1||surgery:1||survival analysis:1||synteny:1||transacting:1||triglycerides:1||trio:1||ulcerative colitis:1||variomics:1||visualiza:1||web service:1||#8217:1||whole genome association study:1||16S rRNA sequencing:1||5Methylcytosine:1||ARM:1||AUC:1||Alternative splicing:1||Arachidonate binding mode:1||Association rule mining:1||Atopic dermatitis:1||BAC end library:1||BLAST analysis:1||Big data:1||Bone mineral density:1||Boolean network:1||CHARGE:1||CNV:1||CSMD1:1||Carnivorous diet:1||Cell type annotation:1||Chromatin signature:1||Chronic kidney disease:1||Classification:1||

STATISTICS: Total View :7,897,180; Today View :2,644

RSS_1.0 RSS_2.0 ATOM_1.0

Soongsil University Library 369 Sangdo-Ro, Dongjak-Gu, Seoul, Korea (06978)02-820-0733

Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.

Detailed Information

Keyword

BROWSE