Gene amplification of the transcription factor DP1 and the CTNND1 in human lung cancer

Acquired chromosome abnormalities in the lungs of patients with Pulmonary Arterial Hypertension (Illumina)

An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer

The relationship between DNA methylation, genetic and expression inter-individual variation in untransformed human fibroblasts

Exonic variants associated with development of Aspirin Exacerbated Respiratory Diseases

A large germline alteration affecting MAX and FUT8, causing familial bilateral malignant pheochromocytoma and renal oncocytoma

Copy number variation of human intestinal stem cells with different passage in culture (two pedigrees, passage 5, 10, 15 and 20)

Copy number variation of human intestinal stem cells with different passage in culture (five pedifrees, passage 5 and 25)

Cloning and Variation of Ground State Intestinal Stem Cells Super [expression & SNP studies]

The UBC-40 Urothelial Bladder Cancer Cell Line Index [copy number variation]

The UBC-40 Urothelial Bladder Cancer Cell Line Index

Chromosomal microarray analysis for validation of the NGS-based CNV detection results in clinical samples

Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples

Copy number variation analysis of human Barrett's esophagus stem cells (HumanOmniZhongHua-8 v1.0 Beadchip)

Copy number variation analysis of human Barrett's esophagus stem cells (HumanOmniZhongHua-8 v1.1 Beadchip)

Copy number variation analysis of human Barrett's esophagus stem cells

Infinium 850k Beadchip analysis of control human brain for copy number mosaicism

Modifying DNA extraction protocol alters human brain copy number estimation

Genome-wide association study on craniofacial microsomia

Combined Genetic and Genealogic Studies Uncover a Large BAP1 Cancer Syndrome Kindred Tracing Back Nine Generations to a Common Ancestor from the 1700s.