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Volumn 23, Issue 7, 2015, Pages 975-983

Rare variant genotype imputation with thousands of study-specific whole-genome sequences: Implications for cost-effective study designs

(26)  Pistis, Giorgio a,b,c   Porcu, Eleonora a,b,c   Vrieze, Scott I b   Sidore, Carlo a,b,c   Steri, Maristella a   Danjou, Fabrice a   Busonero, Fabio a,b   Mulas, Antonella a,c   Zoledziewska, Magdalena a   Maschio, Andrea a,b   Brennan, Christine d   Lai, Sandra a   Miller, Michael B e   Marcelli, Marco f   Urru, Maria Francesca f   Pitzalis, Maristella a   Lyons, Robert H d   Kang, Hyun M b   Jones, Chris M f   Angius, Andrea a,d   more..


Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANCESTRY GROUP; ARTICLE; CHROMOSOME 20; COMPARATIVE EFFECTIVENESS; COST EFFECTIVENESS ANALYSIS; EUROPEAN; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; GENOTYPE IMPUTATION; GENOTYPING TECHNIQUE; HUMAN; NORMAL HUMAN; PRACTICE GUIDELINE; PRIORITY JOURNAL; UNITED STATES; CAUCASIAN; COST BENEFIT ANALYSIS; DNA SEQUENCE; ECONOMICS; GENETICS; GENOME-WIDE ASSOCIATION STUDY; HAPLOTYPE; HUMAN GENOME; ITALY; METHODOLOGY; MINNESOTA; POPULATION GENETICS; PROCEDURES; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84930868547     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2014.216     Document Type: Article
Times cited : (81)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.