HIGHLIGHTS
- who: Marina Sirota from the Background and Summary In the last decade, the advent and continued development of genotyping and next-generation sequencing technologies has enabled researchers to generate a vast amount of molecular dataThe current and evergrowing availability of public ‘omics' databases, including Gene Expression Omnibus1, Array Express3, dbGAP4, and numerous other repositories, along with computational tools to reveal molecular drivers of disease at a network level, present a unique and new opportunity to refine current knowledge about disease mechanisms, diagnostics, and therapeutics. In addition, novel technologies are allowing highthroughput measurements of the human genome, epigenome . . .

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