(Q30558760)

13 August 2017

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

1 reference

13 August 2017

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3

Suzanne M Leal

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13 August 2017

Biao Li

1

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13 August 2017

Gao Wang

series ordinal

2

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13 August 2017

language of work or name

English

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publication date

22 August 2012

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13 August 2017

2

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based on heuristic

inferred from page(s)

published in

Bioinformatics

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13 August 2017

28

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13 August 2017

20

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13 August 2017

2703-2704

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

13 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

Simulating sequences of the human genome with rare variants

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

A map of human genome variation from population-scale sequencing

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

Pooled association tests for rare variants in exon-resequencing studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

A survey of genetic simulation software for population and epidemiological studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

simuPOP: a forward-time population genetics simulation environment

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3467746

10.1093/BIOINFORMATICS/BTS499

14 July 2018

Identifiers

DOI

1 reference

journals/bioinformatics/LiWL12

13 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

13 August 2017

PubMed publication ID

22914216

1 reference