The sharing of genomic data holds great promise in advancing precision medicine and
providing personalized treatments and other types of interventions. However, these …

Accessing and integrating human genomic data with phenotypes are important for
biomedical research. Making genomic data accessible for research purposes, however …

We are entering an era of ubiquitous genetic information for research, clinical care and
personal curiosity. Sharing these data sets is vital for progress in biomedical research …

As the scale of genomic and health-related data explodes and our understanding of these
data matures, the privacy of the individuals behind the data is increasingly at stake …

Recent developments in a variety of sectors, including health care, research and the direct-
to-consumer industry, have led to a dramatic increase in the amount of genomic data that …

The generation of functional genomics data by next-generation sequencing has increased
greatly in the past decade. Broad sharing of these data is essential for research …

The study of human genomics is becoming a Big Data science, owing to recent
biotechnological advances leading to availability of millions of personal genome sequences …

Genome sequencing technology has advanced at a rapid pace and it is now possible to
generate highly-detailed genotypes inexpensively. The collection and analysis of such data …

Motivation: Increased availability of various genotyping techniques has initiated a race for
finding genetic markers that can be used in diagnostics and personalized medicine …

Fulfilling the promise of the genetic revolution requires the analysis of large datasets
containing information from thousands to millions of participants. However, sharing human …