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Association studies for next-generation sequencing
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
title
Association studies for next-generation sequencing
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
author
Eric Boerwinkle
series ordinal
2
object named as
Eric Boerwinkle
0 references
author name string
Li Luo
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
Momiao Xiong
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
publication date
26 April 2011
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
published in
Genome Research
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
volume
21
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
page(s)
1099-1108
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
issue
7
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
cites work
To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
retrieved
8 July 2018
Statistical analysis strategies for association studies involving rare variants
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Pooled association tests for rare variants in exon-resequencing studies
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Accurate detection and genotyping of SNPs utilizing population sequencing data
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Rare variants create synthetic genome-wide associations
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Population genetic inference from genomic sequence variation
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PubMed Central
reference URL
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8 July 2018
Detecting rare variants for complex traits using family and unrelated data
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8 July 2018
Finding the missing heritability of complex diseases
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8 July 2018
Common vs. rare allele hypotheses for complex diseases
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
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PubMed Central
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8 July 2018
Evaluation of next generation sequencing platforms for population targeted sequencing studies
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Human genetic variation and its contribution to complex traits
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Estimation of allele frequencies from high-coverage genome-sequencing projects
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes
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8 July 2018
A groupwise association test for rare mutations using a weighted sum statistic
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
The prevalence of folate-remedial MTHFR enzyme variants in humans
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Accounting for bias from sequencing error in population genetic estimates
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
A comparison of bayesian methods for haplotype reconstruction from population genotype data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
retrieved
8 July 2018
Generating samples under a Wright-Fisher neutral model of genetic variation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
The probability distribution of the amount of an individual's genome surviving to the following generation
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
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8 July 2018
De novo fragment assembly with short mate-paired reads: Does the read length matter?
1 reference
stated in
PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
retrieved
27 September 2018
The distribution of rare alleles.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129252
retrieved
27 September 2018
Identifiers
DOI
10.1101/GR.115998.110
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
PMCID
3129252
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
PubMed ID
21521787
1 reference
stated in
Europe PubMed Central
PubMed ID
21521787
retrieved
6 August 2017
ResearchGate publication ID
51078612
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