A systematic survey of loss-of-function variants in human protein-coding genes by MacArthur, D, Balasubramanian, S, Frankish, A, Huang, N, Morris, J, Walter, K, Jostins, L, Habegger, L, Pickrell, J, Montgomery, S, Albers, C, Zhang, Z, Conrad, D, Lunter, G, Zheng, H, Ayub, Q, DePristo, M, Banks, E, Hu, M, Handsaker, R, Rosenfeld, J, Fromer, M, Jin, M, Mu, X, Khurana, E

A systematic survey of loss-of-function variants in human protein-coding genes. by MacArthur, D, Balasubramanian, S, Frankish, A, Huang, N, Morris, J, Walter, K, Jostins, L, Habegger, L, Pickrell, J, Montgomery, S, Albers, C, Zhang, Z, Conrad, D, Lunter, G, Zheng, H, Ayub, Q, DePristo, M, Banks, E, Hu, M, Handsaker, R, Rosenfeld, J, Fromer, M, Jin, M, Mu, X, Khurana, E

Pathway and network analysis of more than 2500 whole cancer genomes by Reyna, MA, Haan, D, Paczkowska, M, Verbeke, LPC, Vazquez, M, Kahraman, A, Pulido-Tamayo, S, Barenboim, J, Wadi, L, Dhingra, P, Shrestha, R, Getz, G, Lawrence, MS, Pedersen, JS, Rubin, MA, Wheeler, DA, Brunak, S, Izarzugaza, JMG, Khurana, E, Marchal, K, von Mering, C, Sahinalp, SC, Valencia, A, PCAWG Drivers and Functional Interpretation Working Group, Reimand, J, Stuart, JM, Raphael, BJ, PCAWG Consortium

Mapping copy number variation by population-scale genome sequencing. by Mills, R, Walter, K, Stewart, C, Handsaker, R, Chen, K, Alkan, C, Abyzov, A, Yoon, S, Ye, K, Cheetham, R, Chinwalla, A, Conrad, D, Fu, Y, Grubert, F, Hajirasouliha, I, Hormozdiari, F, Iakoucheva, L, Iqbal, Z, Kang, S, Kidd, J, Konkel, M, Korn, J, Khurana, E, Kural, D, Lam, H, Leng, J, Li, R, Li, Y, Lin, C, Luo, R, Mu, X, Nemesh, J, Peckham, H, Rausch, T, Scally, A, Shi, X, Stromberg, M, Stütz, A, Urban, A, Walker, J, Wu, J, Zhang, Y, Zhang, Z, Batzer, M, Ding, L, Marth, G, McVean, G, Sebat, J, Snyder, M, Wang, J, Ye, K, Eichler, E, Gerstein, M, Hurles, M, Lee, C, McCarroll, SA, Korbel, J