Search Results - Paxton Reed
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O33: Concordance of long-read genome sequencing with methylation calling with clinical testing for individuals with Prader-Willi or Angelman Syndrome* by Cate Paschal, Anita Beck, Madelyn Gillentine, Jaya Narayanan, Paxton Reed, Miranda Galey, Danny Miller
Published in Genetics in Medicine Open (2023-01-01)Get full text
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3-hour genome sequencing and targeted analysis to rapidly assess genetic risk by Miranda P.G. Zalusky, Jonas A. Gustafson, Stephanie C. Bohaczuk, Ben Mallory, Paxton Reed, Tara Wenger, Erika Beckman, Irene J. Chang, Cate R. Paschal, Jillian G. Buchan, Christina M. Lockwood, Mihai Puia-Dumitrescu, Daniel R. Garalde, Joseph Guillory, Androo J. Markham, Michael J. Bamshad, Evan E. Eichler, Andrew B. Stergachis, Danny E. Miller
Published in Genetics in Medicine Open (2024-01-01)Get full text
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