(Q47301717)

13 January 2018

title

Principal component analysis for selection of optimal SNP-sets that capture intragenic genetic variation (English)

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13 January 2018

principal component analysis

main subject

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2

Nicola J Camp

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13 January 2018

author name string

Benjamin D Horne

series ordinal

1

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13 January 2018

publication date

1 January 2004

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13 January 2018

published in

Genetic Epidemiology

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13 January 2018

volume

26

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13 January 2018

issue

1

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13 January 2018

page(s)

11-21

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13 January 2018

Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

Variations on a theme: cataloging human DNA sequence variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

An analysis of linkage disequilibrium in the interleukin-1 gene cluster, using a novel grouping method for multiallelic markers.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

High-resolution haplotype structure in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

The structure of haplotype blocks in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Haplotype tagging for the identification of common disease genes

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Efficient selective screening of haplotype tag SNPs

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

The new genomics: global views of biology

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Searching for genetic determinants in the new millennium

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Candidate-gene approaches for studying complex genetic traits: practical considerations

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Evolution of the simulated data problem.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

HaploBlockFinder: haplotype block analyses

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10292

7 January 2021

Identifiers

DOI

10.1002/GEPI.10292

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13 January 2018

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13 January 2018