A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth and senescence escape via regulation of MITF

A comprehensively characterized cell line panel highly representative of clinical ovarian high-grade serous carcinomas

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

A robust machine learning approach for missing persons cases with high genotyping errors

AUTS2 project

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

African American hepatocyte genotype

An Integrated Epigenomic and Genomic View on Phyllodes and Phyllodes-like Breast Tumors

Analysis of Whole Genome Sequence and Genome-wide SNPs in Highly Inbred Pigs [Array]

CEP55 is a determinant of cell fate during perturbed mitosis in breast cancer

Cancer Associated Fibroblasts are defined by a core set of epigenome changes that contribute to the tumor phenotype

Cancer Associated Fibroblasts are defined by a core set of epigenome changes that contribute to the tumor phenotype [Illumina_Omini 2.5-8_SNP]

Candidate driver genes in Sѐzary syndrome

Characterization of a novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient

Characterization of a novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient [Genotype]

Chromosomal aberrations associated with sequential steps of the metastatic cascade in colorectal cancer patients

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

Clonal Evolution of Acute Myeloid Leukemia Revealed by High-Throughput Single-Cell Genomics

Clonal variation in drug and radiation response among glioma-initiating cells is linked to proneural-mesenchymal transition