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Whole genome sequencing
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
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]
- ↑ 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.
- ↑ Mullin, Emily. "Patients face a frustrating diagnostic odyssey when genome sequencing doesn't provide an answer". MIT Technology Review. Retrieved March 29, 2019.
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