Quantitative trait locus analysis for next-generation sequencing with the functional linear models. (Q36495652)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

title

Quantitative trait locus analysis for next-generation sequencing with the functional linear models (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

main subject

quantitative trait locus

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Li Luo

1 reference

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11 February 2020

Momiao Xiong

series ordinal

1 reference

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11 February 2020

language of work or name

English

0 references

publication date

1 August 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

11 February 2020

published in

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11 February 2020

volume

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11 February 2020

issue

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11 February 2020

page(s)

513-524

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Epigenome-wide association studies for common human diseases

11 February 2020

cites work

1 reference

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Rare-variant association testing for sequencing data with the sequence kernel association test

30 September 2017

1 reference

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Optimum designs for next-generation sequencing to discover rare variants for common complex disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Common functional principal components analysis: a new approach to analyzing human movement data.

30 September 2017

1 reference

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Association studies for next-generation sequencing

30 September 2017

1 reference

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Testing for an unusual distribution of rare variants

30 September 2017

1 reference

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A new testing strategy to identify rare variants with either risk or protective effect on disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Bayesian analysis of rare variants in genetic association studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

An evolutionary framework for association testing in resequencing studies.

30 September 2017

1 reference

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Comprehensive Approach to Analyzing Rare Genetic Variants

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

A Novel Adaptive Method for the Analysis of Next-Generation Sequencing Data to Detect Complex Trait Associations with Rare Variants Due to Gene Main Effects and Interactions

30 September 2017

1 reference

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Statistical analysis strategies for association studies involving rare variants

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Pooled association tests for rare variants in exon-resequencing studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

A data-adaptive sum test for disease association with multiple common or rare variants

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Understanding mechanisms underlying human gene expression variation with RNA sequencing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Transcriptome genetics using second generation sequencing in a Caucasian population

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Population genetic inference from genomic sequence variation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Sequencing technologies - the next generation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

An evaluation of statistical approaches to rare variant analysis in genetic association studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Association tests using kernel-based measures of multi-locus genotype similarity between individuals

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Estimation of allele frequencies from high-coverage genome-sequencing projects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

A groupwise association test for rare mutations using a weighted sum statistic

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Using Wavelet-Based Functional Mixed Models to Characterize Population Heterogeneity in Accelerometer Profiles: A Case Study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Accounting for bias from sequencing error in population genetic estimates

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Generating samples under a Wright-Fisher neutral model of genetic variation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

Comparison of methods and sampling designs to test for association between rare variants and quantitative traits.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

De novo fragment assembly with short mate-paired reads: Does the read length matter?

21 September 2018

1 reference

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The distribution of rare alleles.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851

10.1136/JMEDGENET-2012-100798

21 September 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

PubMed publication ID

22889854

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json