Author:
Frankish Adam,Uszczynska Barbara,Ritchie Graham RS,Gonzalez Jose M,Pervouchine Dmitri,Petryszak Robert,Mudge Jonathan M,Fonseca Nuno,Brazma Alvis,Guigo Roderic,Harrow Jennifer
Publisher
Springer Science and Business Media LLC
Reference37 articles.
1. Genomes Project C, Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA: An integrated map of genetic variation from 1,092 human genomes. Nature. 2012, 491 (7422): 56-65. 10.1038/nature11632.
2. UK10K: Rare Genetic Variants in Health and Disease (2010-2013). [ http://www.uk10k.org ]
3. Futema M, Plagnol V, Li K, Whittall RA, Neil HA, Seed M, Simon Broome C, Bertolini S, Calandra S, Descamps OS, et al: Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations. J Med Genet. 2014, 51 (8): 537-544. 10.1136/jmedgenet-2014-102405.
4. Fu W, O'Connor TD, Jun G, Kang HM, Abecasis G, Leal SM, Gabriel S, Rieder MJ, Altshuler D, Shendure J, et al: Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants. Nature. 2013, 493 (7431): 216-220.
5. 100,000 Genomes Project. [ http://www.genomicsengland.co.uk ]
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