A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis
出版年份 2015 全文链接
标题
A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis
作者
关键词
-
出版物
BIOINFORMATICS
Volume 31, Issue 9, Pages 1452-1459
出版商
Oxford University Press (OUP)
发表日期
2015-01-08
DOI
10.1093/bioinformatics/btu860
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Utilizing Population Controls in Rare-Variant Case-Parent Association Tests
- (2014) Yu Jiang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
- (2014) Dalila Pinto et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits
- (2014) Paul L Auer et al. NATURE GENETICS
- The multifunctional Staufen proteins: conserved roles from neurogenesis to synaptic plasticity
- (2014) Jacki E. Heraud-Farlow et al. TRENDS IN NEUROSCIENCES
- Haplotype Estimation Using Sequencing Reads
- (2013) Olivier Delaneau et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rare-Variant Extensions of the Transmission Disequilibrium Test: Application to Autism Exome Sequence Data
- (2013) Zongxiao He et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Parental Broader Autism Subphenotypes in ASD Affected Families: Relationship to Gender, Child's Symptoms, SSRI Treatment, and Platelet Serotonin
- (2013) Tal Levin-Decanini et al. Autism Research
- Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
- (2013) A. Jeremy Willsey et al. CELL
- Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
- (2013) Carlos Cruchaga et al. NATURE
- Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders
- (2013) Elaine T. Lim et al. NEURON
- Rare Variant Analysis for Family-Based Design
- (2013) Gourab De et al. PLoS One
- Genotype calling and haplotyping in parent-offspring trios
- (2012) W. Chen et al. GENOME RESEARCH
- Differential confounding of rare and common variants in spatially structured populations
- (2012) Iain Mathieson et al. NATURE GENETICS
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- (2012) J. A. Tennessen et al. SCIENCE
- An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People
- (2012) M. R. Nelson et al. SCIENCE
- A Likelihood-Based Framework for Variant Calling and De Novo Mutation Detection in Families
- (2012) Bingshan Li et al. PLoS Genetics
- INCREASING POWER BY USING HAPLOTYPE SIMILARITY IN A MULTIMARKER TRANSMISSION/DISEQUILIBRIUM TEST
- (2012) MARÍA M. ABAD-GRAU et al. Journal of Bioinformatics and Computational Biology
- Characterization of a 8q21.11 Microdeletion Syndrome Associated with Intellectual Disability and a Recognizable Phenotype
- (2011) María Palomares et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Spatio-temporal transcriptome of the human brain
- (2011) Hyo Jung Kang et al. NATURE
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- The importance of phase information for human genomics
- (2011) Ryan Tewhey et al. NATURE REVIEWS GENETICS
- Testing for an Unusual Distribution of Rare Variants
- (2011) Benjamin M. Neale et al. PLoS Genetics
- Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
- (2010) Alkes L. Price et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rare Variant Association Analysis Methods for Complex Traits
- (2010) Jennifer Asimit et al. Annual Review of Genetics
- MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
- (2010) Yun Li et al. GENETIC EPIDEMIOLOGY
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- A Data-Adaptive Sum Test for Disease Association with Multiple Common or Rare Variants
- (2010) Fang Han et al. HUMAN HEREDITY
- Variance component model to account for sample structure in genome-wide association studies
- (2010) Hyun Min Kang et al. NATURE GENETICS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- 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
- (2010) Dajiang J. Liu et al. PLoS Genetics
- A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals
- (2009) Brian L. Browning et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Bayesian statistical methods for genetic association studies
- (2009) Matthew Stephens et al. NATURE REVIEWS GENETICS
- Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
- (2009) S. Nejentsev et al. SCIENCE
- A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
- (2009) Bo Eskerod Madsen et al. PLoS Genetics
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data
- (2008) Bingshan Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Maximizing association statistics over genetic models
- (2008) Juan R. González et al. GENETIC EPIDEMIOLOGY
- Rare independent mutations in renal salt handling genes contribute to blood pressure variation
- (2008) Weizhen Ji et al. NATURE GENETICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now