(Q31125474)

29 June 2017

title

Simulating association studies: a data-based resampling method for candidate regions or whole genome scans (English)

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29 June 2017

main subject

whole genome sequencing

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8

Patrick F Sullivan

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29 June 2017

9

Kirk C Wilhelmsen

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29 June 2017

Fred A Wright

1

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29 June 2017

Hanwen Huang

2

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29 June 2017

Xiaojun Guan

3

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29 June 2017

Kevin Gamiel

4

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29 June 2017

Clark Jeffries

5

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29 June 2017

William T Barry

6

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29 June 2017

Fernando Pardo-Manuel de Villena

7

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29 June 2017

Fei Zou

10

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29 June 2017

language of work or name

English

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publication date

4 September 2007

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29 June 2017

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29 June 2017

volume

23

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29 June 2017

issue

19

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29 June 2017

page(s)

2581-2588

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A haplotype map of the human genome

29 June 2017

cites work

1 reference

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Haplotype interaction analysis of unlinked regions.

21 January 2018

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Genetic signatures of strong recent positive selection at the lactase gene

21 January 2018

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Haplotype evolution and linkage disequilibrium: A simulation study

21 January 2018

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Ascertainment bias in studies of human genome-wide polymorphism.

21 January 2018

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Efficiency and power in genetic association studies

21 January 2018

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Linkage disequilibrium mapping in isolated populations: the example of Finland revisited

21 January 2018

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Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies

21 January 2018

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The ENCODE (ENCyclopedia Of DNA Elements) Project

21 January 2018

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The International HapMap Project

21 January 2018

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An empirical comparison of case-control and trio based study designs in high throughput association mapping

21 January 2018

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Genome-wide association studies for common diseases and complex traits

21 January 2018

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Unraveling heterochromatin

21 January 2018

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SIMCOAL 2.0: a program to simulate genomic diversity over large recombining regions in a subdivided population with a complex history.

21 January 2018

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Searching for disease-susceptibility loci by testing for Hardy-Weinberg disequilibrium in a gene bank of affected individuals.

21 January 2018

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A case study of the utility of the HapMap database for pharmacogenomic haplotype analysis in the Taiwanese population

21 January 2018

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Multilocus LD measure and tagging SNP selection with generalized mutual information

21 January 2018

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

21 January 2018

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Cost-effective analysis of candidate genes using htSNPs: a staged approach

21 January 2018

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The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis

21 January 2018

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The effects of human population structure on large genetic association studies

21 January 2018

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Genome-wide strategies for detecting multiple loci that influence complex diseases.

21 January 2018

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A comparison of phasing algorithms for trios and unrelated individuals

21 January 2018

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Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

21 January 2018

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HapSim: a simulation tool for generating haplotype data with pre-specified allele frequencies and LD coefficients

21 January 2018

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A fine-scale map of recombination rates and hotspots across the human genome

21 January 2018

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Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene

21 January 2018

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Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus

21 January 2018

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Simulations provide support for the common disease-common variant hypothesis

21 January 2018

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Forward-time simulations of human populations with complex diseases

21 January 2018

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Simulating haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

Principal components analysis corrects for stratification in genome-wide association studies

21 January 2018

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https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

The allelic architecture of human disease genes: common disease-common variant... or not?

21 January 2018

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Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes

21 January 2018

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The future of genetic studies of complex human diseases

21 January 2018

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Two-stage designs for gene-disease association studies with sample size constraints

21 January 2018

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Calibrating a coalescent simulation of human genome sequence variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

Robustness of inference of haplotype block structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

Mapping by admixture linkage disequilibrium: advances, limitations and guidelines

21 January 2018

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A comparison of bayesian methods for haplotype reconstruction from population genotype data

21 January 2018

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A map of the human genome in linkage disequilibrium units.

21 January 2018

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https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

Recent human effective population size estimated from linkage disequilibrium

21 January 2018

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Recent developments in genomewide association scans: a workshop summary and review

21 January 2018

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A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping

21 January 2018

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Convergent adaptation of human lactase persistence in Africa and Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

In silico analysis of disease-association mapping strategies using the coalescent process and incorporating ascertainment and selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

Validity of tagging SNPs across populations for association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTM386

10.1093/BIOINFORMATICS/BTM386

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/WrightHGGJBVSWZ07

29 June 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference