Exome Sequencing Raises Hopes of Improved Diagnoses and Patient Care

[TECH NEWS]

In the June 13 issue of Science Translational Medicine, an international team led by researchers from the University of California, San Diego School of Medicine reports that the new technology of exome sequencing is not only a promising method for identifying disease-causing genes, but may also improve diagnoses and guide individual patient care. In exome sequencing, researchers selectively and simultaneously target and map all of the portions of the genome where exons reside. Exons are short, critical sequences of DNA in genes that are translated into proteins – the biological workhorses involved in virtually every cellular function, plus various structural or mechanical duties. The researchers, headed by principal investigator Joseph G. Gleeson, MD, sequenced the exomes of 118 patients who had been diagnosed with specific neurodevelopmental diseases. In each of the cases, all known genetic causes of their disease had been previously excluded. Not surprisingly, the scientists found that exome sequencing newly identified numerous disease-causing genes.

 June 13, 2012, University of California San Diego School of Medicine