(Q39345468)

11 September 2017

title

Rare variant association test in family-based sequencing studies (English)

1 reference

11 September 2017

1 reference

11 September 2017

Christopher A Walsh

1 reference

11 September 2017

Xihong Lin

1 reference

11 September 2017

Tianxi Cai

1 reference

11 September 2017

Xuefeng Wang

1 reference

11 September 2017

Zhenyu Zhang

1 reference

11 September 2017

Nathan Morris

1 reference

11 September 2017

Seunggeun Lee

1 reference

11 September 2017

Chaolong Wang

1 reference

11 September 2017

publication date

26 September 2016

1 reference

Briefings in Bioinformatics

11 September 2017

published in

1 reference

A New Method for Detecting Associations with Rare Copy-Number Variants

11 September 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Improved ancestry estimation for both genotyping and sequencing data using projection procrustes analysis and genotype imputation

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Greater power and computational efficiency for kernel-based association testing of sets of genetic variants

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Two-phase and family-based designs for next-generation sequencing studies

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Robust rare variant association testing for quantitative traits in samples with related individuals

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

GEE-based SNP set association test for continuous and discrete traits in family-based association studies

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

A powerful and efficient set test for genetic markers that handles confounders

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Adjusted sequence kernel association test for rare variants controlling for cryptic and family relatedness.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Test for interactions between a genetic marker set and environment in generalized linear models

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Family-based association tests for sequence data, and comparisons with population-based association tests

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Sequence kernel association test for quantitative traits in family samples

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

On the relative efficiency of using summary statistics versus individual-level data in meta-analysis

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

SNP set association analysis for familial data

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Optimal tests for rare variant effects in sequencing association studies

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

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

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

CONVERGENCE AND PREDICTION OF PRINCIPAL COMPONENT SCORES IN HIGH-DIMENSIONAL SETTINGS.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Data quality control in genetic case-control association studies.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Comparing spatial maps of human population-genetic variation using Procrustes analysis

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Working-correlation-structure identification in generalized estimating equations.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Worldwide human relationships inferred from genome-wide patterns of variation

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

A unified association analysis approach for family and unrelated samples correcting for stratification.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Family-based association tests for genomewide association scans

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Calibrating a coalescent simulation of human genome sequence variation

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Hypothesis testing in semiparametric additive mixed models

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Akaike's information criterion in generalized estimating equations.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Asymptotic bias and efficiency in case-control studies of candidate genes and gene-environment interactions: basic family designs

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

Testing association between candidate-gene markers and phenotype in related individuals, by use of estimating equations

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5862290

journals/bib/WangZMCLWYWL17

1 October 2018

Identifiers

DOI

10.1093/BIB/BBW083

0 references

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

release_jnavnlfbrvh6lagh5nstfkwfv4

28 January 2021

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jnavnlfbrvh6lagh5nstfkwfv4

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

5862290

0 references

1 reference