Literature DB >> 26177964

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

Biao Li1, Gao T Wang1, Suzanne M Leal1.   

Abstract

MOTIVATION: There is great interest in analyzing next generation sequence data that has been generated for pedigrees. However, unlike for population-based data there are only a limited number of rare variant methods to analyze pedigree data. One limitation is the ability to evaluate type I and II errors for family-based methods, due to lack of software that can simulate realistic sequence data for pedigrees.
SUMMARY: We developed RarePedSim (Rare-variant Pedigree-based Simulator), a program to simulate region/gene-level genotype and phenotype data for complex and Mendelian traits for any given pedigree structure. Using a genetic model, sequence variant data can be generated either conditionally or unconditionally on pedigree members' qualitative or quantitative phenotypes. Additionally, qualitative or quantitative traits can be generated conditional on variant data. Sequence data can either be simulated using realistic population demographic models or obtained from sequence-based studies. Variant sites can be annotated with positions, allele frequencies and functionality. For rare variants, RarePedSim is the only program that can efficiently generate both genotypes and phenotypes, regardless of pedigree structure. Data generated by RarePedSim are in standard Linkage file (.ped) and Variant Call (.vcf) formats, ready to be used for a variety of purposes, including evaluation of type I error and power, for association methods including mixed models and linkage analysis methods.
AVAILABILITY AND IMPLEMENTATION: bioinformatics.org/simped/rare CONTACT: sleal@bcm.edu.
© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Mesh:

Year:  2015        PMID: 26177964      PMCID: PMC4757949          DOI: 10.1093/bioinformatics/btv412

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


  11 in total

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Review 4.  Family-based designs for genome-wide association studies.

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5.  Collapsed haplotype pattern method for linkage analysis of next-generation sequence data.

Authors:  Gao T Wang; Di Zhang; Biao Li; Hang Dai; Suzanne M Leal
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Review 8.  Statistical analysis strategies for association studies involving rare variants.

Authors:  Vikas Bansal; Ondrej Libiger; Ali Torkamani; Nicholas J Schork
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9.  SeqSIMLA: a sequence and phenotype simulation tool for complex disease studies.

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  5 in total

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Journal:  Am J Hum Genet       Date:  2017-01-05       Impact factor: 11.025

2.  SimRVSequences: an R package to simulate genetic sequence data for pedigrees.

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Journal:  Bioinformatics       Date:  2020-04-01       Impact factor: 6.937

3.  Simulating autosomal genotypes with realistic linkage disequilibrium and a spiked-in genetic effect.

Authors:  M Shi; D M Umbach; A S Wise; C R Weinberg
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4.  A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data.

Authors:  Linhai Zhao; Zongxiao He; Di Zhang; Gao T Wang; Alan E Renton; Badri N Vardarajan; Michael Nothnagel; Alison M Goate; Richard Mayeux; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2019-10-03       Impact factor: 11.025

5.  Comparative assessment of different familial aggregation methods in the context of large and unstructured pedigrees.

Authors:  Christian X Weichenberger; Johannes Rainer; Cristian Pattaro; Peter P Pramstaller; Francisco S Domingues
Journal:  Bioinformatics       Date:  2019-01-01       Impact factor: 6.937

  5 in total

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