Illumina SNP and CNV data for the HuRef individual

Genotyping SAX1 Mouse Human Hybrid

ENPP1 deletion and infantile arterial calcification

Generation and Characterization of an immortalized human mesenchymal stromal cell line model [Affymetrix]

aCGH of chromosome X in a female patient with ALL and Leri-Weill syndrome

Detection of CNVs in patients with syndromic intellectual disability

Functional interrogation of twenty Type 2 Diabetes-associated genes using isogenic hESC-derived β-like cells (SNP chip)

U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line

Genotyping data from one patient with unexplained mental retardation and a deletion in 15q13

Homozygosity mapping in a consanguineous family with osteogenesis imperfecta (OI)

Genotyping human lymphoblastoid cell lines

Emergence of Non-Random Chromosomal Alterations (Trisomy 7 and 20) Derived from Diploid Human Colonic Epithelial Cells

LIF-Dependent, Pluripotent Stem Cells Established from Inner Cell Mass of Porcine Embryos

Pediatric Hepatocellular Carcinoma Celll Line

Chromothripsis in AML

Overexpression of mutant EGFR (E746-A750del) enhances the tumourigenic properties of MCF10CA1a cells

Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring [case 2]

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

Affymetrix Mouse Diversity Genotyping Array for 129S2/SvPasCrl and 129S4/SvJae

Genome-wide copy number profiling of MCF-7 and fulvestrant-resistant MCF-7/FR cells by SNP microarray.