Detalhe da pesquisa
1.
Development of the variant calling algorithm, ADIScan, and its use to estimate discordant sequences between monozygotic twins.
Nucleic Acids Res
; 46(15): e92, 2018 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29873758
2.
Integrated genome sizing (IGS) approach for the parallelization of whole genome analysis.
BMC Bioinformatics
; 19(1): 462, 2018 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30509173
3.
HLAscan: genotyping of the HLA region using next-generation sequencing data.
BMC Bioinformatics
; 18(1): 258, 2017 May 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28499414
4.
Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia.
BMC Med Genet
; 18(1): 23, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28249600
5.
Genetic characterization of porcine epidemic diarrhea virus in Korea from 1998 to 2013.
Arch Virol
; 160(4): 1055-64, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25666198
6.
Novel COL9A3 mutation in a family diagnosed with multiple epiphyseal dysplasia: a case report.
BMC Musculoskelet Disord
; 15: 371, 2014 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25381065
7.
Proteomic and bioinformatic analysis of membrane proteome in type 2 diabetic mouse liver.
Proteomics
; 13(7): 1164-79, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23349036
8.
Nitrosylation of ß2-Tubulin Promotes Microtubule Disassembly and Differentiated Cardiomyocyte Beating in Ischemic Mice.
Tissue Eng Regen Med
; 20(6): 921-937, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37679590
9.
RDscan: A New Method for Improving Germline and Somatic Variant Calling Based on Read Depth Distribution.
J Comput Biol
; 29(9): 987-1000, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35749140
10.
Deep learning model enables the discovery of a novel immunotherapeutic agent regulating the kynurenine pathway.
Oncoimmunology
; 10(1): 2005280, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34858729
11.
Planning the human variome project: the Spain report.
Hum Mutat
; 30(4): 496-510, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19306394
12.
A Mutation in ZNF143 as a Novel Candidate Gene for Endothelial Corneal Dystrophy.
J Clin Med
; 8(8)2019 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31390831
13.
Cancer Drug Response Profile scan (CDRscan): A Deep Learning Model That Predicts Drug Effectiveness from Cancer Genomic Signature.
Sci Rep
; 8(1): 8857, 2018 06 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29891981
14.
Correction to: Nitrosylation of ß2-Tubulin Promotes Microtubule Disassembly and Differentiated Cardiomyocyte Beating in Ischemic Mice.
Tissue Eng Regen Med
; 20(7): 1219, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37938524
15.
Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.
BMC Med Genet
; 8: 70, 2007 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-18036257
16.
Prevalence of Rare Genetic Variations and Their Implications in NGS-data Interpretation.
Sci Rep
; 7(1): 9810, 2017 08 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-28851938
17.
Structural and functional analyses of mutations of the human phenylalanine hydroxylase gene.
Clin Chim Acta
; 365(1-2): 279-87, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16253218
18.
Differential expression of MicroRNAs in patients with glioblastoma after concomitant chemoradiotherapy.
OMICS
; 17(5): 259-68, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23586679
19.
Gene flow between the Korean peninsula and its neighboring countries.
PLoS One
; 5(7): e11855, 2010 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-20686617
20.
Mapping human genetic diversity in Asia.
Science
; 326(5959): 1541-5, 2009 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-20007900