SCOPUS 정보 검색 플랫폼

BMC Proceedings

Volumn 5, Issue SUPPL. 9, 2011, Pages

Evaluating methods for the analysis of rare variants in sequence data

(6) Luedtke, Alexander a Powers, Scott b Petersen, Ashley c Sitarik, Alexandra d Bekmetjev, Airat e Tintle, Nathan L e

a BROWN UNIVERSITY (United States)

b University of North Carolina at Chapel Hill (United States)

c ST OLAF COLLEGE (United States)

d WITTENBERG UNIVERSITY (United States)

e DORDT COLLEGE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONFERENCE PAPER; GENE FREQUENCY; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENOTYPE; INTERMETHOD COMPARISON; MATHEMATICAL MODEL; MEDICAL RESEARCH; MULTIVARIATE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS;

EID: 82455199497 PISSN: None EISSN: 17536561 Source Type: Journal
DOI: 10.1186/1753-6561-5-S9-S119 Document Type: Conference Paper

Times cited : (16)

References (7)

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2
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- Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data
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- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Li B, Leal SM, Am J Hum Genet 2008 83 311 321 10.1016/j.ajhg.2008.06.024 18691683
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- Li, B.¹ Leal, S.M.²

3
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- An evaluation of statistical approaches to rare variant analysis in genetic association studies
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- Morris, A.¹ Zeggini, E.²

4
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- Extending rare variant testing strategies: Analysis of non-coding sequence and imputed genotypes
- 10.1016/j.ajhg.2010.10.012 21070896
- Extending rare variant testing strategies: analysis of non-coding sequence and imputed genotypes. Zawistowski M, Gopalakrishnan S, Ding J, Li Y, Grimm S, Zollner S, Am J Hum Genet 2010 87 604 617 10.1016/j.ajhg.2010.10.012 21070896
- (2010) Am J Hum Genet , vol.87 , pp. 604-617
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6
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- Statistical analysis of rare sequence variants: An overview of collapsing methods
- Statistical analysis of rare sequence variants: an overview of collapsing methods. Dering C, Pugh E, Ziegler A, Genet Epidemiol 2011 3 Suppl 8 12 17
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7
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