Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Genome-wide detection of recurring sites of uniparental disomy in folicular and transformed follicular lymphoma

Frequent Partial Uniparental Disomy Due to Somatic Recombination in Acute Myeloid Leukemias

SCLC cell line profiling on 100K arrays

Genomic profiling data of 40 childhood leukemia patients

SNP array analysis of chromosomal instability patterns discriminates rectal adenomas from carcinomas

Pancreatic cancer_Affymetrix 100K SNP arrays

SNPchip analysis of single cell products

Structural Variation of Chromosomes in Autism Spectrum Disorder.

comparison of HL60-NG cell and HL60-RG cell

Copy Number Analysis of Renal Epithelial Neoplasms

SNP-based mapping and gene expression profiling identifies novel chromosomal imbalances and candidate genes in T-PLL

High-resolution genetic analysis of cancer cell lines with near normal karyotypes

Genome wide genotyping and gene expression data of childhood B-cell precursor ALL without known genetic aberrations

Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia

Genomic profiling of TP53 and non-TP53 Li-Fraumeni syndrome tumors reveals hits in the p53 and overlapping pathways

Chromophobe and Oncocytoma Renal Cell Carcinomas: gene expression and SNP analysis

Analysis of copy number change in cord lining epithelial cells after phage integrase mediated genomic integration.

Optimizations of DNA isolation and copy number analysis identifies regions of genomic gain/loss in early breast cancer

SNP data from Neuroblastoma samples