Reprogramming of Human Fibroblasts into Hematopoietic Progenitors by Fusion With Human Fetal Liver CD34+ Cells

Epigenome signatures during gastric carcinogenesis based on next generation sequencing

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

SCLC cell line profiling on 100K arrays

Pancreatic cancer_Affymetrix 100K SNP arrays

Genomic profiling data of 40 childhood leukemia patients

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

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

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

SNPchip analysis of single cell products

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

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

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

Structural Variation of Chromosomes in Autism Spectrum Disorder.

Copy Number Analysis of Renal Epithelial Neoplasms

comparison of HL60-NG cell and HL60-RG cell

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

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