Pan-genomic study of primary human retinoblastoma samples

miR-181a initiates and perpetuates oncogenic transformation through the regulation of innate immune signaling (genomic Variation dataset)

Genome-wide association study of body weights in Hu sheep

Establishment and characterization of testicular cancer patient-derived xenograft (PDX) models [SNP array]

The evolution of MET and NRAS gene amplification as sequential acquired resistance mechanisms in a patient with EGFR mutation positive non-small cell lung cancer

Human HFF cells large rearrangements detection after CRISPR-Cas9 nuclease (Supplentary Fig. 4)

Hereditary Hearing Loss SNP-Microarray Pilot Study

Genome-Wide Association Study Towards Genomic Predictive Power for High Production and Quality of Milk in American Alpine Goats

Mechanisms and disease associations of haplotype-dependent allele specific DNA methylation

Systems genomics study reveals expression quantitative trait loci, regulator genes and pathways associated with boar taint in pigs (SNP60v2 BeadChip data set)

Genome-wide single nucleotide polymorphism array and whole-genome sequencing reveal the inbreeding progression of Banna minipig inbred line

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

Preclinical quality, safety and efficacy of a human embryonic stem cell-derived product for treatment of people with moderate Parkinson’s Disease (STEM-PD)

Preimplantation Genetic Testing Analysis for a Chinese Family with Hereditary Spherocytosis Caused by a Novel Splicing Variant of SPTB

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

Gene amplification of the transcription factor DP1 and the CTNND1 in human lung cancer

SNP array for CNV calling AUTS2 project [Illumina]

AUTS2 project

The relationship between DNA methylation, genetic and expression inter-individual variation in untransformed human fibroblasts

Genome wide DNA copy number analysis of sarcomatoid renal cell carcinoma.