Literature DB >> 22914216

SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.

Biao Li1, Gao Wang, Suzanne M Leal.   

Abstract

MOTIVATION: Currently, there is great interest in detecting complex trait rare variant associations using next-generation sequence data. On a monthly basis, new rare variant association methods are published. It is difficult to evaluate these methods because there is no standard to generate data and often comparisons are biased. In order to fairly compare rare variant association methods, it is necessary to generate data using realistic population demographic and phenotypic models. RESULT: SimRare is an interactive program that integrates generation of rare variant genotype/phenotype data and evaluation of association methods using a unified platform. Variant data are generated for gene regions using forward-time simulation that incorporates realistic population demographic and evolutionary scenarios. Phenotype data can be obtained for both case-control and quantitative traits. SimRare has a user-friendly interface that allows for easy entry of genetic and phenotypic parameters. Novel rare variant association methods implemented in R can also be imported into SimRare, to evaluate their performance and compare results, e.g. power and Type I error, with other currently available methods both numerically and graphically.

Mesh:

Year:  2012        PMID: 22914216      PMCID: PMC3467746          DOI: 10.1093/bioinformatics/bts499

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  12 in total

1.  Simulating sequences of the human genome with rare variants.

Authors:  Bo Peng; Xiaoming Liu
Journal:  Hum Hered       Date:  2011-01-06       Impact factor: 0.444

2.  Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.

Authors:  Ivan P Gorlov; Olga Y Gorlova; Shamil R Sunyaev; Margaret R Spitz; Christopher I Amos
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

3.  Power of deep, all-exon resequencing for discovery of human trait genes.

Authors:  Gregory V Kryukov; Alexander Shpunt; John A Stamatoyannopoulos; Shamil R Sunyaev
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-06       Impact factor: 11.205

4.  Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.

Authors:  Bingshan Li; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2008-08-07       Impact factor: 11.025

5.  Evolution and functional impact of rare coding variation from deep sequencing of human exomes.

Authors:  Jacob A Tennessen; Abigail W Bigham; Timothy D O'Connor; Wenqing Fu; Eimear E Kenny; Simon Gravel; Sean McGee; Ron Do; Xiaoming Liu; Goo Jun; Hyun Min Kang; Daniel Jordan; Suzanne M Leal; Stacey Gabriel; Mark J Rieder; Goncalo Abecasis; David Altshuler; Deborah A Nickerson; Eric Boerwinkle; Shamil Sunyaev; Carlos D Bustamante; Michael J Bamshad; Joshua M Akey
Journal:  Science       Date:  2012-05-17       Impact factor: 47.728

6.  A map of human genome variation from population-scale sequencing.

Authors:  Gonçalo R Abecasis; David Altshuler; Adam Auton; Lisa D Brooks; Richard M Durbin; Richard A Gibbs; Matt E Hurles; Gil A McVean
Journal:  Nature       Date:  2010-10-28       Impact factor: 49.962

7.  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.

Authors:  Dajiang J Liu; Suzanne M Leal
Journal:  PLoS Genet       Date:  2010-10-14       Impact factor: 5.917

8.  A groupwise association test for rare mutations using a weighted sum statistic.

Authors:  Bo Eskerod Madsen; Sharon R Browning
Journal:  PLoS Genet       Date:  2009-02-13       Impact factor: 5.917

Review 9.  A survey of genetic simulation software for population and epidemiological studies.

Authors:  Youfang Liu; Georgios Athanasiadis; Michael E Weale
Journal:  Hum Genomics       Date:  2008-09       Impact factor: 4.639

10.  Assessing the evolutionary impact of amino acid mutations in the human genome.

Authors:  Adam R Boyko; Scott H Williamson; Amit R Indap; Jeremiah D Degenhardt; Ryan D Hernandez; Kirk E Lohmueller; Mark D Adams; Steffen Schmidt; John J Sninsky; Shamil R Sunyaev; Thomas J White; Rasmus Nielsen; Andrew G Clark; Carlos D Bustamante
Journal:  PLoS Genet       Date:  2008-05-30       Impact factor: 5.917

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  14 in total

1.  Generation of sequence-based data for pedigree-segregating Mendelian or Complex traits.

Authors:  Biao Li; Gao T Wang; Suzanne M Leal
Journal:  Bioinformatics       Date:  2015-07-14       Impact factor: 6.937

Review 2.  Statistical power and significance testing in large-scale genetic studies.

Authors:  Pak C Sham; Shaun M Purcell
Journal:  Nat Rev Genet       Date:  2014-05       Impact factor: 53.242

3.  Gene-set association tests for next-generation sequencing data.

Authors:  Jaehoon Lee; Young Jin Kim; Juyoung Lee; Bong-Jo Kim; Seungyeoun Lee; Taesung Park
Journal:  Bioinformatics       Date:  2016-09-01       Impact factor: 6.937

Review 4.  Identifying rare variants associated with complex traits via sequencing.

Authors:  Bingshan Li; Dajiang J Liu; Suzanne M Leal
Journal:  Curr Protoc Hum Genet       Date:  2013-07

5.  Rare variant association test with multiple phenotypes.

Authors:  Selyeong Lee; Sungho Won; Young Jin Kim; Yongkang Kim; Bong-Jo Kim; Taesung Park
Journal:  Genet Epidemiol       Date:  2016-12-31       Impact factor: 2.135

6.  BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge.

Authors:  Carrie B Moore; John R Wallace; Alex T Frase; Sarah A Pendergrass; Marylyn D Ritchie
Journal:  BMC Med Genomics       Date:  2013-05-07       Impact factor: 3.063

7.  Guidelines for investigating causality of sequence variants in human disease.

Authors:  D G MacArthur; T A Manolio; D P Dimmock; H L Rehm; J Shendure; G R Abecasis; D R Adams; R B Altman; S E Antonarakis; E A Ashley; J C Barrett; L G Biesecker; D F Conrad; G M Cooper; N J Cox; M J Daly; M B Gerstein; D B Goldstein; J N Hirschhorn; S M Leal; L A Pennacchio; J A Stamatoyannopoulos; S R Sunyaev; D Valle; B F Voight; W Winckler; C Gunter
Journal:  Nature       Date:  2014-04-24       Impact factor: 49.962

8.  Cohen's h for detection of disease association with rare genetic variants.

Authors:  Shu-Hui Wen; Jih-I Yeh
Journal:  BMC Genomics       Date:  2014-10-08       Impact factor: 3.969

Review 9.  Exome sequencing and complex disease: practical aspects of rare variant association studies.

Authors:  Ron Do; Sekar Kathiresan; Gonçalo R Abecasis
Journal:  Hum Mol Genet       Date:  2012-09-13       Impact factor: 6.150

10.  SeqSIMLA: a sequence and phenotype simulation tool for complex disease studies.

Authors:  Ren-Hua Chung; Chung-Chin Shih
Journal:  BMC Bioinformatics       Date:  2013-06-20       Impact factor: 3.169

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