Genome-wide SNP Microarray Mapping in Basal Cell Carcinomas Unveils Uniparental Disomy as a Key Somatic Event.

Global variation of copy number in the human genome_EA

Global variation of copy number in the human genome_COMM

SNP array analysis of neuroblastoma tumors

A comparison of DNA copy number profiling platforms using a panel of melanoma cell lines

Structural Variation of Chromosomes in Autism Spectrum Disorder.

The Complete Genome of a Single Individual by Massively Parallel DNA Sequencing

Analysis of genetic changes in MCF10A series cells and MCFDCIS derived xenografts

Adult and adolescent acute lymphoblastic leukemia

Genome-wide analysis of esopageal adenocarcinoma tumor biopsy using high-density single-nucleotide polymorphism arrays.

Focal gains of VEGFA and molecular classification of hepatocellular carcinoma

Copy number alterations of 103 hepatocellular carcinomas with hepatitis C virus etiology

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

Segmentation-based detection of allelic imbalance and LOH in cancer cells using whole genome SNP arrays

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Human ES cells reveal recurrent genomic instability at 20q11.21

Screening for copy-number alterations and LOH in CLL - a comparative study of four microarray platforms

Array CGH analysis in primary human renal tumors, categorized by VHL genotype and HIF-alpha expression

50K SNP Copy Number Analysis of Ovarian Carcinomas