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Year Number of Results
2010 2
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2012 5
2013 4
2014 2
2015 1
2016 1
2024 0

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Page 1
A global reference for human genetic variation.
1000 Genomes Project Consortium; Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, Marchini JL, McCarthy S, McVean GA, Abecasis GR. 1000 Genomes Project Consortium, et al. Nature. 2015 Oct 1;526(7571):68-74. doi: 10.1038/nature15393. Nature. 2015. PMID: 26432245 Free PMC article.
A map of human genome variation from population-scale sequencing.
1000 Genomes Project Consortium; Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA. 1000 Genomes Project Consortium, et al. Nature. 2010 Oct 28;467(7319):1061-73. doi: 10.1038/nature09534. Nature. 2010. PMID: 20981092 Free PMC article.
Haplotype estimation using sequencing reads.
Delaneau O, Howie B, Cox AJ, Zagury JF, Marchini J. Delaneau O, et al. Am J Hum Genet. 2013 Oct 3;93(4):687-96. doi: 10.1016/j.ajhg.2013.09.002. Am J Hum Genet. 2013. PMID: 24094745 Free PMC article.
HAPGEN2: simulation of multiple disease SNPs.
Su Z, Marchini J, Donnelly P. Su Z, et al. Bioinformatics. 2011 Aug 15;27(16):2304-5. doi: 10.1093/bioinformatics/btr341. Epub 2011 Jun 8. Bioinformatics. 2011. PMID: 21653516 Free PMC article.
Genotype imputation with thousands of genomes.
Howie B, Marchini J, Stephens M. Howie B, et al. G3 (Bethesda). 2011 Nov;1(6):457-70. doi: 10.1534/g3.111.001198. Epub 2011 Nov 1. G3 (Bethesda). 2011. PMID: 22384356 Free PMC article.
Reference-based phasing using the Haplotype Reference Consortium panel.
Loh PR, Danecek P, Palamara PF, Fuchsberger C, A Reshef Y, K Finucane H, Schoenherr S, Forer L, McCarthy S, Abecasis GR, Durbin R, L Price A. Loh PR, et al. Nat Genet. 2016 Nov;48(11):1443-1448. doi: 10.1038/ng.3679. Epub 2016 Oct 3. Nat Genet. 2016. PMID: 27694958 Free PMC article.
16 results