(Q42636999)

English

Information capture using SNPs from HapMap and whole-genome chips differs in a sample of inflammatory and cardiovascular gene-centric regions from genome-wide estimates

scientific article published on 25 September 2007

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

Information capture using SNPs from HapMap and whole-genome chips differs in a sample of inflammatory and cardiovascular gene-centric regions from genome-wide estimates (English)

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

whole genome sequencing

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

object named as

Richard J Dobson

2

0 references

object named as

Mark J Caulfield

4

0 references

Patricia B Munroe

3

object named as

Patricia B Munroe

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

publication date

25 September 2007

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Europe PubMed Central

PMC publication ID

4 November 2017

Genome Research

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Europe PubMed Central

PMC publication ID

4 November 2017

17

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

11

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

1596-1602

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

Coverage and power in genomewide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

Biases and reconciliation in estimates of linkage disequilibrium in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

A haplotype map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

Sequence features in regions of weak and strong linkage disequilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

Efficiency and power in genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

The ENCODE (ENCyclopedia Of DNA Elements) Project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

Initial sequencing and analysis of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

dbSNP: the NCBI database of genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

A greedy algorithm for aligning DNA sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

27 May 2018

Evaluating coverage of genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

16 August 2018

Evaluating and improving power in whole-genome association studies using fixed marker sets.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

16 August 2018

Common deletion polymorphisms in the human genome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

16 August 2018

Alu-associated enhancement of single nucleotide polymorphisms in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

16 August 2018

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

1 December 2018

Comparison of human genetic and sequence-based physical maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2045142

1 December 2018

Identifiers

10.1101/GR.5996407

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

ResearchGate publication ID

0 references

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