Mutation discovery in mice by whole exome sequencing
- Fairfield, H; Gilbert, GJ; Barter, M; Corrigan, RR; Curtain, M; Ding, YM; D'Ascenzo, M; Gerhardt, DJ; He, C; Huang, WH; Richmond, T; Rowe, L; Probst, FJ; Bergstrom, DE; Murray, SA; Bult, C; Richardson, J; Kile, BT; Gut, I; Hager, J; Sigurdsson, S; Mauceli, E; Di Palma, F; Lindblad-Toh, K; Cunningham, ML; Cox, TC; Justice, MJ; Spector, MS; Lowe, SW; Albert, T; Donahue, LR; Jeddeloh, J; Shendure, J; Reinholdt, LG;
Publication Year 2011, Volume 12, Issue #9, Page -
- Journal Title
- GENOME BIOLOGY
- Publication Type
- Journal Article
- We report the development and optimization of reagents for in-solution, hybridization-based capture of the mouse exome. By validating this approach in a multiple inbred strains and in novel mutant strains, we show that whole exome sequencing is a robust approach for discovery of putative mutations, irrespective of strain background. We found strong candidate mutations for the majority of mutant exomes sequenced, including new models of orofacial clefting, urogenital dysmorphology, kyphosis and autoimmune hepatitis.
- BIOMED CENTRAL LTD
- BALANCER CHROMOSOME; HEARING-LOSS; MOUSE
- Publisher's Version
- Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2011-01-01 12:00:00Last Modified: 0001-01-01 12:00:00