Whole exome sequencing

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Whole exome sequencing (WES) is a form of genetic testing that maps all of a person's exons, pieces of DNA that provide instructions for making proteins.[1] The human exome (complete set of exons) is thought to make up one percent of the human genome.[1] Whole genome sequencing (WGS), which maps the full genome, is more costly and most mutations known to cause diseases are found in the exome, so mapping the exome has provided a comparatively affordable yet effective improvement on previous testing that only mapped a select few genes.[1] Recently, though, costs for WGS have decreased, becoming closer to the price of WES; in 2017, researcher Liz Worthey's lab charged $6,500 for WGS, versus $5,000 to $5,500 for WES.[2] Additionally, WGS may be preferable as some genetic disorders are caused by mutations outside the exome, meaning WES would not detect them. At the same time, the medical and research value of the large quantities of information generated by WGS remains uncertain, given many genetic variations do not cause illness.[1]

See also[edit | edit source]

References[edit | edit source]

  1. 1.0 1.1 1.2 1.3 "What are whole exome sequencing and whole genome sequencing?". Genetics Home Reference. U.S. National Library of Medicine. Retrieved January 13, 2019.
  2. Mullin, Emily. "Patients face a frustrating diagnostic odyssey when genome sequencing doesn't provide an answer". MIT Technology Review. Retrieved March 29, 2019.

The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.