(Q35187645)

7 August 2017

title

Simulating sequences of the human genome with rare variants (English)

1 reference

7 August 2017

Bo Peng

1

1 reference

7 August 2017

Xiaoming Liu

series ordinal

2

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7 August 2017

publication date

1 January 2010

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7 August 2017

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7 August 2017

volume

70

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7 August 2017

issue

4

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7 August 2017

page(s)

287-291

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Forward-time simulation of realistic samples for genome-wide association studies

7 August 2017

cites work

1 reference

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Pooled association tests for rare variants in exon-resequencing studies

28 July 2018

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Rare variants create synthetic genome-wide associations

28 July 2018

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Common vs. rare allele hypotheses for complex diseases

28 July 2018

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28 July 2018

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

28 July 2018

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A survey of genetic simulation software for population and epidemiological studies

28 July 2018

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A flexible forward simulator for populations subject to selection and demography

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164177

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28 July 2018

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

28 July 2018

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ForSim: a tool for exploring the genetic architecture of complex traits with controlled truth

28 July 2018

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

28 July 2018

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Common and rare variants in multifactorial susceptibility to common diseases

28 July 2018

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GENOMEPOP: a program to simulate genomes in populations

28 July 2018

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Sequence-level population simulations over large genomic regions

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164177

Forward-time simulations of human populations with complex diseases

28 July 2018

1 reference

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Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

28 July 2018

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Simulations provide support for the common disease-common variant hypothesis

28 July 2018

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The distribution of fitness effects of new deleterious amino acid mutations in humans

28 July 2018

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A haplotype map of the human genome

28 July 2018

1 reference

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simuPOP: a forward-time population genetics simulation environment

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164177

Simultaneous inference of selection and population growth from patterns of variation in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164177

SelSim: a program to simulate population genetic data with natural selection and recombination

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164177

Generating samples under a Wright-Fisher neutral model of genetic variation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164177

Uncovering the roles of rare variants in common disease through whole-genome sequencing

28 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1159%2F000323316

GENOME: a rapid coalescent-based whole genome simulator

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1159%2F000323316

21 January 2018

Identifiers

DOI

10.1159/000323316

1 reference

7 August 2017

1 reference

7 August 2017

1 reference