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Association tests and software for copy number variant data
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Association tests and software for copy number variant data
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
author
Vincent Plagnol
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
publication date
1 January 2009
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stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
published in
Human genomics
1 reference
stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
volume
3
1 reference
stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
page(s)
191-194
1 reference
stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
exact match
https://scigraph.springernature.com/pub.10.1186/1479-7364-3-2-191
0 references
cites work
Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease
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14 July 2018
A robust statistical method for case-control association testing with copy number variation
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14 July 2018
Systematic assessment of copy number variant detection via genome-wide SNP genotyping
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14 July 2018
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525277
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14 July 2018
Mapping and sequencing of structural variation from eight human genomes
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PubMed Central
reference URL
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14 July 2018
The fine-scale and complex architecture of human copy-number variation
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PubMed Central
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14 July 2018
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
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14 July 2018
PLINK: a tool set for whole-genome association and population-based linkage analyses
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14 July 2018
Copy-number variation and association studies of human disease
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525277
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14 July 2018
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525277
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14 July 2018
Relative impact of nucleotide and copy number variation on gene expression phenotypes
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PubMed Central
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14 July 2018
Global variation in copy number in the human genome
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14 July 2018
A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase
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14 July 2018
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
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Population structure, differential bias and genomic control in a large-scale, case-control association study
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14 July 2018
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
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14 July 2018
On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1186%2F1479-7364-3-2-191
retrieved
21 January 2018
A high-resolution survey of deletion polymorphism in the human genome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/19164094
retrieved
12 December 2020
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Identifiers
DOI
10.1186/1479-7364-3-2-191
1 reference
stated in
Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
Dimensions Publication ID
1017378983
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release_jbbqsupxejf5jje5243o5uxo5i
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24 November 2022
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PMCID
3525277
1 reference
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Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
PubMed ID
19164094
1 reference
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Europe PubMed Central
PubMed ID
19164094
retrieved
26 July 2017
ResearchGate publication ID
23933262
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