Rare variant association test in family-based sequencing studies (Q39345468)

From Wikidata

Jump to navigation Jump to search

The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

scientific article published on 26 September 2016

Language	Label	Description	Also known as
English	Rare variant association test in family-based sequencing studies	scientific article published on 26 September 2016

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Christopher A. Walsh

8

object named as

Christopher A Walsh

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

9

object named as

Xihong Lin

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

4

object named as

Tianxi Cai

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

author name string

Xuefeng Wang

1

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Zhenyu Zhang

2

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Nathan Morris

3

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Seunggeun Lee

5

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Chaolong Wang

6

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

publication date

26 September 2016

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Briefings in Bioinformatics

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

Sequence kernel association test for quantitative traits in family samples

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

SNP set association analysis for familial data

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

Optimal tests for rare variant effects in sequencing association studies

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

Data quality control in genetic case-control association studies.

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

Working-correlation-structure identification in generalized estimating equations.

1 reference

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

1 October 2018

Worldwide human relationships inferred from genome-wide patterns of variation

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

Family-based association tests for genomewide association scans

1 reference

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

1 October 2018

Calibrating a coalescent simulation of human genome sequence variation

1 reference

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

1 October 2018

Hypothesis testing in semiparametric additive mixed models

1 reference

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

1 October 2018

Akaike's information criterion in generalized estimating equations.

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

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

1 reference

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

1 October 2018

Identifiers

10.1093/BIB/BBW083

0 references

DBLP publication ID

journals/bib/WangZMCLWYWL17

1 reference

DBLP Dataset 2021-01-02

28 January 2021

release_jnavnlfbrvh6lagh5nstfkwfv4

1 reference

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

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q39345468&oldid=1835770077"