Somatic copy number variants in monozygotic twins and elderly single-born individuals

Illumina HapMap YRI (HumanCNV100Wv1.0)

Genomic approach in B-cell Chronic Lymphocytic Leukemia: molecularly distinct subgroups of patients with 13q14 deletion

Identification of MicroRNA Expression Patterns and a MicroRNAs/mRNA Regulatory Network in Multiple Myeloma

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

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

Genetic Association study of Autism in Saudi Females using SNP array

Genome-Wide Association Study of Hospitalized COVID-19 Patients in the United Arab Emirates

Dynamic Changes in the Copy Number of Pluripotency and Cell Proliferation Genes in Human ES and iPS Cells during Reprogramming and Time in Culture

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

Key Super Enhancers Drive Tumor-Suppressing Transcription Feedback Programs in Mature B Cell Cancers (SNP array)

Key Super Enhancers Drive Tumor-Suppressing Transcription Feedback Programs in Mature B Cell Cancers

Illumina SNP array data for acute myeloid leukemia samples

Genetic variants associated with coronary artery disease in Indians

Kazak mitochondrial genomes provide insights into the human population history of Central Eurasia

The self-renewal of gastric cancer stem cells is regulated by a specific collaboration between the microenvironment and the genetic condition.

Affymetrix SNP array data for beak deformity and normal Beijing-You Chickens

Genome alterations in human pluripotent stem cells as very early events highly dependent on cell passaging conditions

A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33

Comparison of Cancer-Associated Genetic Abnormalities in Columnar-Lined Esophagus with and without Goblet Cells