Scientists finally read the hidden DNA code that shapes disease
EMBL researchers created SDR-seq, a next-generation tool that decodes both DNA and RNA from the same cell. It finally opens access to non-coding regions, where most disease-associated genetic variants lie. By revealing how these variants affect gene activity, scientists can better understand complex diseases and develop improved diagnostic tools.

For centuries, scientists have noticed that certain illnesses seem to pass from one generation to the next, a connection first noted by Hippocrates, who observed that some diseases "ran in families." Over time, researchers have steadily advanced their ability to uncover the biological roots of these inherited patterns within the human genome.
A team of EMBL researchers and collaborators has now created a tool that takes single-cell analysis to a new level. It can capture both genomic variations and RNA within the same cell, offering greater accuracy and scalability than earlier…




