(Q35751969)

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Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis

scientific article published on January 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

10 August 2017

Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis (English)

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Europe PubMed Central

PubMed publication ID

10 August 2017

genome-wide association study

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lessons learned

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based on heuristic

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whole genome sequencing

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based on heuristic

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Andreas Ziegler

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Andreas Ziegler

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Alexander F Wilson

1

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Europe PubMed Central

PubMed publication ID

10 August 2017

publication date

1 January 2011

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Europe PubMed Central

PubMed publication ID

10 August 2017

Genetic Epidemiology

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Europe PubMed Central

PubMed publication ID

10 August 2017

35 Suppl 1

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Europe PubMed Central

PubMed publication ID

10 August 2017

S107-14

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Europe PubMed Central

PubMed publication ID

10 August 2017

Digging into the extremes: a useful approach for the analysis of rare variants with continuous traits?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Comparing nominal and real quality scores on next-generation sequencing genotype calls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Genetic Analysis Workshop 17 mini-exome simulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Rare variants, common markers: synthetic association and beyond

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Incorporating linkage information into a common disease/rare variant framework

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Multiple testing in high-throughput sequence data: experiences from Group 8 of Genetic Analysis Workshop 17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Analysis of exome sequences with and without incorporating prior biological knowledge.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Incorporating biological information into association studies of sequencing data.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Quality control issues and the identification of rare functional variants with next-generation sequencing data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Detecting multiple causal rare variants in exome sequence data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Effect of linkage disequilibrium on the identification of functional variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Identification of genetic association of multiple rare variants using collapsing methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Application of the regression of offspring on mid-parent method to detect associations between single-nucleotide polymorphisms and the beta 2 electroencephalogram phenotype in the COGA data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

2 October 2017

Population-based and family-based designs to analyze rare variants in complex diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277851

12 July 2018

Dealing with high dimensionality for the identification of common and rare variants as main effects and for gene-environment interaction.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20659

21 January 2018

Comparison of variance components, ANOVA and regression of offspring on midparent (ROMP) methods for SNP markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/22128050

12 December 2020

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10.1002/GEPI.20659

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

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