Phasing for medical sequencing using rare variants and large haplotype reference panels by Sharp, K, Kretzschmar, W, Delaneau, O, Marchini, J

Methods for transcription and forced alignment of a legacy speech corpus by Olsen, R, Olsen, M, Stanley, J, Renwick, M, Kretzschmar, W

A reference panel of 64,976 haplotypes for genotype imputation by Kretzschmar, W, Mahajan, A, Sharp, K, McCarthy, M, Haplotype Reference Consortium

11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project. by Cai, N, Bigdeli, T, Kretzschmar, W, Li, Y, Liang, J, Hu, J, Peterson, R, Bacanu, S, Webb, B, Riley, B, Li, Q, Marchini, J, Mott, R, Kendler, K, Flint, J

Genomic partitioning and cross-population polygene scoring of major depressive disorder in N=11,651 Han Chinese women using low-pass sequencing data by Bigdeli, T, Edwards, A, Peterson, R, Li, Y, Kretzschmar, W, Yang, F, Maes, H, Fanous, A, Webb, B, Riley, B, Wang, J, Shi, S, Chen, Y, Marchini, J, Mott, R, Bacanu, S, Flint, J, Kendler, K

Functional parameters derived from magnetic resonance imaging reflect vascular 1 morphology in preclinical tumors and in human liver metastases by Kannan, P, Kretzschmar, W, Winter, H, Warren, D, Bates, R, Allen, P, Syed, N, Irving, B, Papiez, B, Kaeppler, J, Markelc, B, Kinchesh, P, Gilchrist, S, Smart, S, Schnabel, J, Maughan, T, Harris, A, Muschel, R, Partridge, M, Sharma, R, Kersemans, V

Accelerated RNA splicing dynamics during erythroid differentiation amplify mis-splicing in SF3B1-mutant MDS-RS by Mead, A, Moura, P, Mortera-Blanco, T, Hofman, I, Todisco, G, Kretzschmar, W, Bjorklund, A-C, Creignou, M, Hagemann-Jensen, M, Ziegenhain, C, Granados, D, Barbosa, I, Walldin, G, Jansson, M, Lundin, V, Dimitriou, M, Yoshizato, T, Woll, P, Ogawa, S, Sandberg, R, Jacobsen, SE, Hellstrom-Lindberg, E