Detecting multiple causal rare variants in exome sequence data.
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Considering interactive effects in the identification of influential regions with extremely rare variants via fixed bin approachLessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysisThe value of extended pedigrees for next-generation analysis of complex disease in the rhesus macaque
P2860
Detecting multiple causal rare variants in exome sequence data.
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2011 nî lūn-bûn
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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年學術文章
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Detecting multiple causal rare variants in exome sequence data.
@ast
Detecting multiple causal rare variants in exome sequence data.
@en
Detecting multiple causal rare variants in exome sequence data.
@nl
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label
Detecting multiple causal rare variants in exome sequence data.
@ast
Detecting multiple causal rare variants in exome sequence data.
@en
Detecting multiple causal rare variants in exome sequence data.
@nl
prefLabel
Detecting multiple causal rare variants in exome sequence data.
@ast
Detecting multiple causal rare variants in exome sequence data.
@en
Detecting multiple causal rare variants in exome sequence data.
@nl
P2860
P356
P1433
P1476
Detecting multiple causal rare variants in exome sequence data.
@en
P2093
Corinne D Engelman
Kenny Q Ye
P2860
P304
P356
10.1002/GEPI.20644
P478
35 Suppl 1
P577
2011-01-01T00:00:00Z