Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

PUBLICATION DATE

13 results
Display

A Clinical Risk Score to Predict In-hospital Mortality from COVID-19 in South Korea

Her AY, Bhak Y, Jun EJ, Yuan SL, Garg S, Lee S, Bhak J, Shin ES

Background: Early identification of patients with coronavirus disease 2019 (COVID-19) who are at high risk of mortality is of vital importance for appropriate clinical decision making and delivering optimal treatment....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
New Lung Cancer Panel for High-Throughput Targeted Resequencing

Kim EH, Lee S, Park J, Lee K, Bhak J, Kim BC

We present a new next-generation sequencing-based method to identify somatic mutations of lung cancer. It is a comprehensive mutation profiling protocol to detect somatic mutations in 30 genes found frequently...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Post-GWAS Strategies

Kim S, Bhak J

  • KMID: 1450879
  • Genomics Inform.
  • 2011 Mar;9(1):1-4.
Genome-wide association (GWA) studies are the method of choice for discovering loci associated with common diseases. More than a thousand GWA studies have reported successful identification of statistically significant association...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
How Many SNPs Should Be Used for the Human Phylogeny of Highly Related Ethnicities? A Case of Pan Asian 63 Ethnicities

Ghang H, Han Y, Jeong S, Bhak J, Lee S, Kim TH, Kim C, Kim S, Al-Mulla F, Youn CH, Yoo HS, The HUGO Pan-Asian SNP Consortium

  • KMID: 2053274
  • Genomics Inform.
  • 2011 Dec;9(4):181-188.
In planning a model-based phylogenic study for highly related ethnic data, the SNP marker number is an important factor to determine for relationship inferences. Genotype frequency data, utilizing a sub...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Structural Bioinformatics Analysis of Disease-related Mutations

Park SJ, Oh S, Park D, Bhak J

  • KMID: 2166411
  • Genomics Inform.
  • 2008 Sep;6(3):142-146.
In order to understand the protein functions that are related to disease, it is important to detect the correlation between amino acid mutations and isease. Many mutation studies about disease-related...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Personal Genomics, Bioinformatics, and Variomics

Bhak J, Ghang H, Reja R, Kim S

  • KMID: 2166415
  • Genomics Inform.
  • 2008 Dec;6(4):161-165.
In 2008 at least five complete genome sequences are available. It is known that there are over 15,000,000 genetic variants, called SNPs, in the dbSNP database. The cost of full...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Biological Object Downloader (BOD) Service for Easy Download and Management of Biological Databases

Park D, Lee J, Yoon G, Gong S, Bhak J

  • KMID: 2166287
  • Genomics Inform.
  • 2007 Dec;5(4):196-199.
BOD is an FTP service management tool on the Internet. It was developed for biological researchers in South Korea. It enables easier and faster access of bioinformation without having to...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
BioCC: An Openfree Hypertext Bio Community Cluster for Biology

Gong S, Kim TH, Oh J, Kwon J, Cho SA, Bolser D, Bhak J

  • KMID: 1512147
  • Genomics Inform.
  • 2006 Sep;4(3):125-128.
We present an openfree hypertext (also known as wiki) web cluster called BioCC. BioCC is a novel wiki farm that lets researchers create hundreds of biological web sites. The web...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
HExDB: Human EXon DataBase for Alternative Splicing Pattern Analysis

Park J, Lee M, Bhak J

  • KMID: 1572678
  • Genomics Inform.
  • 2005 Sep;3(3):80-85.
HExDB is a database for analyzing exon and splicing pattern information in Homo sapiens. HExDB is useful for specific purposes: 1) to design primers for exon amplification from cDNA and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
BioCovi: A Visualization Service for Comparative Genomics Analysis

Lee J, Park D, Bhak J

  • KMID: 1572632
  • Genomics Inform.
  • 2005 Jun;3(2):52-54.
Visualization of the homology information is an important method to analyze the evolutionary and functional meanings of genes. With a database containing model genomes of Homo sapiens, Mus muculus, and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
BioSubroutine: an Open Web Server for Bioinformatics Algorithms and Subroutines

Lee J, Kim H, Lee W, Chung D, Bhak J

  • KMID: 1572619
  • Genomics Inform.
  • 2005 Mar;3(1):35-38.
We present BioSubroutine, an open depository server that automatically categorizes various subroutines frequently used in bioinformatics research. We processed a large bioinformatics subroutine library called Bio.pl that was the first...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
High Correlation between Alu Elements and the Conversion of 3' UTR of mRNAs Processed Pseudogenes

An HJ, Na D, Lee D, Lee KH, Bhak J

  • KMID: 2166170
  • Genomics Inform.
  • 2004 Jun;2(2):86-91.
Even though it represents 6 13% of human genomic DNA, Alu sequences are rarely found in coding regions. When in exon region, over 80 % of them are found in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The Atom of Evolution

Bhak J, Bolser D, Park D, Cho Y, Yoon K, Lee S, Gong S, Jang I, Park C, Huston M, Choi H

  • KMID: 1515373
  • Genomics Inform.
  • 2004 Dec;2(4):167-173.
The main mechanism of evolution is that biological entities change, are selected, and reproduce. We propose a different concept in terms of the main agent or atom of evolution: in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr