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

автор

Xihong Lin

1953 -

David C. Christiani

1951 -

Deborah A Nickerson

1954 - 2021

опубликовано в: American Journal of Human Genetics

дата публикации: 2012-08-02

язык: английский язык

Cites articles 32

Дата

Заголовок

Авторы

2012-07-08

Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

Deborah A Nickerson
2012-06-14

Optimal tests for rare variant effects in sequencing association studies

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2011-07-07

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

Michael C Wu, Michael Boehnke, Xihong Lin, Tianxi Cai
2011-03-03

Testing for an unusual distribution of rare variants

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2010-11-01

Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

David Altshuler, Kristian Cibulskis, Стейси Гэбриел, Aaron McKenna, Mark Joseph Daly, Andrey Sivachenko, Eric Banks, Andrew Kernytsky, Mark DePristo
2010-06-11

Pooled association tests for rare variants in exon-resequencing studies

Alkes Price
2010-04-23

A data-adaptive sum test for disease association with multiple common or rare variants
2010-04

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Peer Bork, Леонид Пешкин
2010-02-01

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Multiple rare alleles contribute to low plasma levels of HDL cholesterol

Alexander Pertsemlidis
2003-07-01

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Статья - wd:Q36152947

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