(Q31020644)

28 June 2017

title

Optimal genotype determination in highly multiplexed SNP data (English)

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28 June 2017

2

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author name string

Martin Moorhead

1

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28 June 2017

Farooq Siddiqui

3

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28 June 2017

Matthew Falkowski

4

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28 June 2017

Carsten Bruckner

5

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28 June 2017

James Ireland

6

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28 June 2017

Hywel B Jones

7

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28 June 2017

Maneesh Jain

8

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28 June 2017

Thomas D Willis

9

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28 June 2017

Malek Faham

10

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28 June 2017

publication date

1 February 2006

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European Journal of Human Genetics

28 June 2017

published in

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28 June 2017

volume

14

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28 June 2017

issue

2

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28 June 2017

page(s)

207-215

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The future of genetic studies of complex human diseases

28 June 2017

cites work

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Multiplexed genotyping with sequence-tagged molecular inversion probes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Large-scale genotyping of complex DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Linkage disequilibrium in humans: models and data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

The structure of haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

What SNP genotyping errors are most costly for genetic association studies?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Population structure, differential bias and genomic control in a large-scale, case-control association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Minimal haplotype tagging

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

The International HapMap Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

inferred from DOI database lookup

7 January 2021

based on heuristic

The impact of genotyping error on haplotype reconstruction and frequency estimation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201528

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201528

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Dimensions Publication ID

28 June 2017

1008259745

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