Identifying rare variants associated with complex traits via sequencing.
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Use of Genomic Tools to Improve Cattle Health in the Context of Infectious DiseasesGenetic variation in IBD: progress, clues to pathogenesis and possible clinical utilityEffective filtering strategies to improve data quality from population-based whole exome sequencing studies.Pooled sequencing and rare variant association tests for identifying the determinants of emerging drug resistance in malaria parasitesA haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysisChoosing Subsamples for Sequencing Studies by Minimizing the Average Distance to the Closest LeafFamily studies to find rare high risk variants in migraine.Population-specific single-nucleotide polymorphism confers increased risk of venous thromboembolism in African Americans.Impact of exome sequencing in inflammatory bowel disease.DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease.Exome-based case-control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy.Exome-wide rare variant analyses of two bone mineral density phenotypes: the challenges of analyzing rare genetic variation.
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Identifying rare variants associated with complex traits via sequencing.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on July 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Identifying rare variants associated with complex traits via sequencing.
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Identifying rare variants associated with complex traits via sequencing.
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type
label
Identifying rare variants associated with complex traits via sequencing.
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Identifying rare variants associated with complex traits via sequencing.
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Identifying rare variants associated with complex traits via sequencing.
@en
Identifying rare variants associated with complex traits via sequencing.
@nl
P2093
P2860
P1476
Identifying rare variants associated with complex traits via sequencing.
@en
P2093
Bingshan Li
Dajiang J Liu
Suzanne M Leal
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P304
P356
10.1002/0471142905.HG0126S78
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P577
2013-07-01T00:00:00Z