네트워크

생명과학

center for Advanced Bioinformatics & Systems Medicine

Databases
MACE
Mutation-oriented analysis of che- mical response in cancer cell lines
GS-LAGE
A novel gene-specific analysis of microarray global data
NetCSSP
Prediction of chameleon seq. and amyloid fibril formation
Tools
Qhelix
Analysis of geometric arrangement
of protein helices
QCanvas
Fast clustering and
visualization of data
Qsurface
Identification of cell surface
transcriptome markers in cancers
line
Smart screening for systems medicines

Availability of multi-level omics data such as genome, transcriptome, proteome and phosphatome data enables system-level analyses for the prediction and characterization of selective drug response on target diseases.

Integration of multi-level omics data with chemical or siRNA screening data on diverse biological samples is accelerating discovery studies on clinically relevant drug applications and their mode of actions.

For this purpose, we have constructed a smart screening platform combining technologies on computer-oriented big data mining and experimental high content screening for last several years.

▶ 1. Pan-omics data mining and screening
dot Method development and optimization for big data analysis
dot Generate diverse patterns and hypotheses describing the association between varied drug
response and molecular signatures such as mutation, gene or protein markers.
dot Validation of target molecules and samples for the optimization of high content siRNA or
chemical library screening
dot
▶ 2. High throughput siRNA and chemical library screening
dot Image and cell-based assay development for high content screening
dot Automation and standardization of high throughput screening
dot System-level interpretation of siRNA library screening
▶ 3. Molecular modeling and drug design
dot Application of machine learning algorithms for cell-based SAR studies
dot 3D shape-based chemical analysis
dot Protein and peptide sequence optimization
dot

국가

대한민국

소속기관

숙명여자대학교 (학교)

연락처

책임자

윤석준 yoonsj@sookmyung.ac.kr

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