Whole genome sequencing

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Whole exome sequencing (WGS) is a form of genetic testing that maps all the nucleotides in a person's DNA, offering the possibility of identifying variations in any part of the genome.[1] As of 2017, researcher Liz Worthey's lab charged $6,500 for WGS.[2]

See also[edit | edit source]

References[edit | edit source]

  1. Reference, Genetics Home. "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.

genome an organism's complete set of DNA, including all of its genes

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.