RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data: Table 1.
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Title
RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data: Table 1.
Authors
Keywords
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Journal
BIOINFORMATICS
Volume 32, Issue 9, Pages 1423-1426
Publisher
Oxford University Press (OUP)
Online
2016-02-16
DOI
10.1093/bioinformatics/btw079
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Note: Only part of the references are listed.- SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations
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- Rare-Variant Association Analysis: Study Designs and Statistical Tests
- (2014) Seunggeung Lee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits
- (2014) Joseph K. Pickrell AMERICAN JOURNAL OF HUMAN GENETICS
- RAREMETAL: fast and powerful meta-analysis for rare variants
- (2014) S. Feng et al. BIOINFORMATICS
- A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data
- (2014) Hao Hu et al. NATURE BIOTECHNOLOGY
- Recommended Joint and Meta-Analysis Strategies for Case-Control Association Testing of Single Low-Count Variants
- (2013) Clement Ma et al. GENETIC EPIDEMIOLOGY
- The Value of Statistical or Bioinformatics Annotation for Rare Variant Association With Quantitative Trait
- (2013) Andrea E. Byrnes et al. GENETIC EPIDEMIOLOGY
- FaST-LMM-Select for addressing confounding from spatial structure and rare variants
- (2013) Jennifer Listgarten et al. NATURE GENETICS
- Meta-analysis of gene-level tests for rare variant association
- (2013) Dajiang J Liu et al. NATURE GENETICS
- A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff
- (2012) Pablo Cingolani et al. FLY
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A probabilistic disease-gene finder for personal genomes
- (2011) M. Yandell et al. GENOME RESEARCH
- FaST linear mixed models for genome-wide association studies
- (2011) Christoph Lippert et al. NATURE METHODS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Power of deep, all-exon resequencing for discovery of human trait genes
- (2009) G. V. Kryukov et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- 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
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