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Rapid clinical diagnostic variant investigation of genomic patient sequencing data with iobio web tools.
Ward, Alistair; Karren, Mary A; Di Sera, Tonya; Miller, Chase; Velinder, Matt; Qiao, Yi; Filloux, Francis M; Ostrander, Betsy; Butterfield, Russell; Bonkowsky, Joshua L; Dere, Willard; Marth, Gabor T.
Affiliation
  • Ward A; Department of Human Genetics, USTAR Center for Genetic Discovery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Karren MA; Department of Human Genetics, USTAR Center for Genetic Discovery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Di Sera T; Department of Human Genetics, USTAR Center for Genetic Discovery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Miller C; Department of Human Genetics, USTAR Center for Genetic Discovery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Velinder M; Department of Human Genetics, USTAR Center for Genetic Discovery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Qiao Y; Department of Human Genetics, USTAR Center for Genetic Discovery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Filloux FM; Department of Pediatrics, Division of Pediatric Neurology, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Ostrander B; Department of Pediatrics, Division of Pediatric Neurology, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Butterfield R; Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Bonkowsky JL; Department of Pediatrics, Division of Pediatric Neurology, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Dere W; Department of Pediatrics, Division of Pediatric Neurology, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
  • Marth GT; Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
J Clin Transl Sci ; 1(6): 381-386, 2017 Dec.
Article in En | MEDLINE | ID: mdl-29707261

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: J Clin Transl Sci Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: J Clin Transl Sci Year: 2017 Document type: Article