Leveraging sequences missing from the human genome to diagnose cancer.

Georgakopoulos-Soares I, Yizhar-Barnea O, Mouratidis I, Chan CSY, Patsakis M, Nayak A, Bradley R, Mahajan M, Sims J, Cintron DL, Easterlin R, Kim JS, Chen E, Pineda G, Parada GE, Witte JS, Maher CA, Feng F, Vathiotis I, Syrigos N, Panagiotou E, Charpidou A, Syrigos K, Chapman J, Kvale M, Hemberg M, Ahituv N