Implication of LARS1 Over-expression in Growth and Migration of Lung Cancer Cells by siRNA Targeted Knock-down Analysis.

Comparison of normalization methods for defining copy number variation using whole-genome SNP genotyping data.

CGHscape: A software framework for the detection and visualization of copy number alterations.

Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybrid

Somatic mutations of JAK1 and JAK3 in acute leukemias and solid cancers

Absence of ERCC6 gene mutation in common cancers of Korean patients

Absence of somatic mutation of a tumor suppressor gene eukaryotic translation elongation factor 1, epsilon-1 (EEF1E1), in commo

Copy number variations in the human genome: potential source for individual diversity and disease association studies.

Tumor suppressor WTX gene mutation is rare in acute leukemias.

유전체복제수 변이(CNV)와 당뇨병

CD63 as a biomarker for predicting the clinical outcomes in adenocarcinoma of lung.

Inferring biological functions and associated transcriptional regulators using gene set expression coherence analysis.

Germline methylation patterns inferred from local nucleotide frequency of repetitive sequences in the human genome.

Recurrent genomic alterations with impact on survival in colorectal cancer identified by genome-wide array comparative genomic

Gene expression signatures associated with the resistance to imatinib.