Rare genetic variants in noncoding regions of the human genome can cause severe rare disease 1,2, but their role in common, complex traits is still largely unknown. Array-based imputation, genome-wide ...

The advent of high-throughput sequencing uncovered that our genome is pervasively transcribed into RNAs that are seemingly not translated into proteins. It was also found that non-coding RNA ...

In just a few decades, DNA sequencing technologies evolved from slow, manual processes to rapid, automated ones, making ...