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Structural haplotypes and recent evolution of the human 17q21.31 region

Boettger, L. M. et al.

Nature genetics. VOL 44; NUMBER 8, ; 2012, 881-885 -- Nature Publishing Group Part 8; (pages 881-885) -- 2012

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Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

Handsaker, R. E. et al.

Nature genetics. VOL 43; NUMBER 3, ; 2011, 269-276 -- Nature Publishing Group -- 2011

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Mapping the Human Reference Genome’s Missing Sequence by Three-Way Admixture in Latino Genomes

Genovese, G. et al.

American journal of human genetics. VOL 93; NUMBER 3, ; 2013, 411-421 -- Elsevier Science B.V., Amsterdam Part 3; (pages 411-421) -- 2013

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Genetic Variation in Human DNA Replication Timing

Koren, A. et al.

Cell. VOL 159; NUMBER 5, ; 2014, 1015-1026 -- Elsevier Science B.V., Amsterdam. Part 5; (pages 1015-1026) -- 2014

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Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels

Boettger, L. M. et al.

Nature genetics. VOL 48; NUMBER 4, ; 2016, 359-366 -- Nature Publishing Group (pages 359-366) -- 2016

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Large multiallelic copy number variations in humans

Handsaker, R. E. et al.

Nature genetics. VOL 47; NUMBER 3, ; 2015, 296-303 -- Nature Publishing Group Part 3; (pages 296-303) -- 2015

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SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

Johnson, A. D. et al.

Bioinformatics. VOL 24; NUMBER 24, ; 2008, 2938-2939 -- Oxford University Press (pages 2938-2939) -- 2008

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Mapping copy number variation by population-scale genome sequencing

Mills, R. E. et al.

Nature. VOL 470; NUMBER 7332, ; 2011, 59-65 -- Nature Publishing Group -- 2011

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Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity

Usher, C. L. et al.

Nature genetics. VOL 47; NUMBER 8, ; 2015, 921-925 -- Nature Publishing Group Part 8; (pages 921-925) -- 2015

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The variant call format and VCFtools

Danecek, P. et al.

Bioinformatics. VOL 27; NUMBER 15, ; 2011, 2156-2158 -- Oxford University Press -- 2011

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