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Autor:
Aleksandra Foksinska, Camerron M. Crowder, Andrew B. Crouse, Jeff Henrikson, William E. Byrd, Gregory Rosenblatt, Michael J. Patton, Kaiwen He, Thi K. Tran-Nguyen, Marissa Zheng, Stephen A. Ramsey, Nada Amin, John Osborne, UAB Precision Medicine Institute, Matthew Might, Stephen Barnes, Mei-Jan Chen, Mary E. Crumbley, Madeline Eckenrode, Crayton A. Fargason, Nathaniel Fehrmann, Forest Huls, Matthew Jarrell, Lindsay Jenkins, Meg McCalley, Tamsyn Osborn, Elizabeth Pollard, Sienna Rucka, Nicholas T. Southern, Jillian Tinglin, Jordan H. Whitlock
Publikováno v:
Frontiers in Artificial Intelligence, Vol 5 (2022)
There are over 6,000 different rare diseases estimated to impact 300 million people worldwide. As genetic testing becomes more common practice in the clinical setting, the number of rare disease diagnoses will continue to increase, resulting in the n
Externí odkaz:
https://doaj.org/article/eafb0ce485144f31abd3b657a1dff8e1
