Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies (Q39817287)

14 September 2017

Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies (English)

1 reference

genome-wide association study

14 September 2017

0 references

author

Vineet Bafna

2

1 reference

14 September 2017

4

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14 September 2017

Bjarni V. Halldórsson

object named as

Bjarni V Halldórsson

1

0 references

author name string

Ross Lippert

3

1 reference

14 September 2017

Francisco M De La Vega

5

1 reference

14 September 2017

Andrew G Clark

6

1 reference

14 September 2017

Sorin Istrail

7

1 reference

14 September 2017

1 August 2004

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14 September 2017

1 reference

14 September 2017

14

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14 September 2017

8

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14 September 2017

1633-1640

1 reference

Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

The International HapMap Project

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Modeling and E-M estimation of haplotype-specific relative risks from genotype data for a case-control study of unrelated individuals

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Assessing the performance of the haplotype block model of linkage disequilibrium

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Minimal haplotype tagging

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Haplotype block partition with limited resources and applications to human chromosome 21 haplotype data

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Efficient selective screening of haplotype tag SNPs

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

A high-resolution recombination map of the human genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

A dynamic programming algorithm for haplotype block partitioning

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

The structure of haplotype blocks in the human genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

The optimal measure of allelic association

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

The impact of SNP density on fine-scale patterns of linkage disequilibrium

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Haplotype tagging single nucleotide polymorphisms and association studies.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Entropy-based SNP selection for genetic association studies

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

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

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Robustness of inference of haplotype block structure.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Selection of minimum subsets of single nucleotide polymorphisms to capture haplotype block diversity.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

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

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Genome scans and candidate gene approaches in the study of common diseases and variable drug responses

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=509273

Haplotype tagging for the identification of common disease genes

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15289481

12 December 2020

inferred from PubMed ID database lookup

The usefulness of different density SNP maps for disease association studies of common variants

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15289481

12 December 2020

inferred from PubMed ID database lookup

Identifiers

1 reference

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30 July 2022

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Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/xb65p3nbqjdelbr3vkue77qwwm

30 July 2022

https://api.fatcat.wiki/v0/release/xb65p3nbqjdelbr3vkue77qwwm

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/xb65p3nbqjdelbr3vkue77qwwm

1 reference

30 July 2022