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Efficiency of whole-exome sequencing in old world and new world primates using human capture reagents.
Chan, Jeannie; Yao, Wen; Howard, Timothy D; Hawkins, Gregory A; Olivier, Michael; Jorgensen, Matthew J; Cheeseman, Ian H; Cole, Shelley A; Cox, Laura A.
Affiliation
  • Chan J; Department of Internal Medicine, Section on Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Yao W; College of Life Sciences, Henan Agricultural University, Zhengzhou, China.
  • Howard TD; Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Hawkins GA; Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Olivier M; Department of Internal Medicine, Section on Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Jorgensen MJ; Department of Pathology, Section on Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Cheeseman IH; Texas Biomedical Research Institute, San Antonio, TX, USA.
  • Cole SA; Texas Biomedical Research Institute, San Antonio, TX, USA.
  • Cox LA; Department of Internal Medicine, Section on Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
J Med Primatol ; 50(3): 176-181, 2021 06.
Article in En | MEDLINE | ID: mdl-33876458
ABSTRACT

BACKGROUND:

Whole-exome sequencing (WES) can expedite research on genetic variation in non-human primate (NHP) models of human diseases. However, NHP-specific reagents for exome capture are not available. This study reports the use of human-specific capture reagents in WES for olive baboons, marmosets, and vervet monkeys.

METHODS:

Exome capture was carried out using the SureSelect Human All Exon V6 panel from Agilent Technologies, followed by high-throughput sequencing. Capture of protein-coding genes and detection of single nucleotide variants were evaluated.

RESULTS:

Exome capture and sequencing results showed that more than 97% of old world and 93% of new world monkey protein coding genes were detected. Single nucleotide variants were detected across the genomes and missense variants were found in genes associated with human diseases.

CONCLUSIONS:

A cost-effective approach based on commercial, human-specific reagents can be used to perform WES for the discovery of genetic variants in these NHP species.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: High-Throughput Nucleotide Sequencing / Exome Limits: Animals / Humans Language: En Journal: J Med Primatol Year: 2021 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: High-Throughput Nucleotide Sequencing / Exome Limits: Animals / Humans Language: En Journal: J Med Primatol Year: 2021 Document type: Article Affiliation country: United States
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