Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.
Saved in:
| Title: | Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases. |
|---|---|
| Authors: | De La Vega, Francisco M.1,2,3 (AUTHOR), Chowdhury, Shimul4 (AUTHOR), Moore, Barry5 (AUTHOR), Frise, Erwin1 (AUTHOR), McCarthy, Jeanette1 (AUTHOR), Hernandez, Edgar Javier5 (AUTHOR), Wong, Terence4 (AUTHOR), James, Kiely4 (AUTHOR), Guidugli, Lucia4 (AUTHOR), Agrawal, Pankaj B.6,7 (AUTHOR), Genetti, Casie A.6 (AUTHOR), Brownstein, Catherine A.6 (AUTHOR), Beggs, Alan H.6 (AUTHOR), Löscher, Britt-Sabina8 (AUTHOR), Franke, Andre8 (AUTHOR), Boone, Braden9 (AUTHOR), Levy, Shawn E.9 (AUTHOR), Õunap, Katrin10,11 (AUTHOR), Pajusalu, Sander10,11 (AUTHOR), Huentelman, Matt12 (AUTHOR) |
| Source: | Genome Medicine. 10/19/2021, Vol. 13 Issue 1, p1-19. 19p. |
| Database: | Academic Search Ultimate |
Be the first to leave a comment!
