Family-based association studies for next-generation sequencing.
about
Progress in methods for rare variant associationAssociation, interaction, and replication analysis of genes encoding serotonin transporter and 5-HT3 receptor subunits A and B in alcohol dependenceTesting genetic association with rare and common variants in family data.Extended T(2) tests for longitudinal family data in whole genome sequencing studies.Detecting multiple variants associated with disease based on sequencing data of case-parent trios.Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data.The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.Application of family-based tests of association for rare variants to pathwaysEvaluation of the power and type I error of recently proposed family-based tests of association for rare variantsA 2-step penalized regression method for family-based next-generation sequencing association studies.Comparison of several sequence-based association methods in pedigreesPatient-controlled encrypted genomic data: an approach to advance clinical genomics.LEVERAGING LOCAL IDENTITY-BY-DESCENT INCREASES THE POWER OF CASE/CONTROL GWAS WITH RELATED INDIVIDUALSTest of rare variant association based on affected sib-pairs.A statistical approach for rare-variant association testing in affected sibshipsGenotype-Based Score Test for Association Testing in Families.Comparing family-based rare variant association tests for dichotomous phenotypes.A novel statistical method for rare-variant association studies in general pedigrees.Prioritization of family member sequencing for the detection of rare variantsA multistep approach to single nucleotide polymorphism-set analysis: an evaluation of power and type I error of gene-based tests of association after pathway-based association testsUncovering Local Trends in Genetic Effects of Multiple Phenotypes via Functional Linear Models.Identification of novel variants in colorectal cancer families by high-throughput exome sequencing.The impact of genotype calling errors on family-based studies.Identifying rare variants associated with complex traits via sequencing.Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.Detecting association of rare variants by testing an optimally weighted combination of variants for quantitative traits in general families.Newborn screening: the genomic challenge.Next generation sequencing and rare genetic variants: from human population studies to medical genetics.Utilising family-based designs for detecting rare variant disease associations.A rare variant association test in family-based designs and non-normal quantitative traits.FARVATX: Family-Based Rare Variant Association Test for X-Linked Genes.Some surprising twists on the road to discovering the contribution of rare variants to complex diseases.Detecting Multiethnic Rare Variants.WISARD: workbench for integrated superfast association studies for related datasets.
P2860
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P2860
Family-based association studies for next-generation sequencing.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Family-based association studies for next-generation sequencing.
@ast
Family-based association studies for next-generation sequencing.
@en
type
label
Family-based association studies for next-generation sequencing.
@ast
Family-based association studies for next-generation sequencing.
@en
prefLabel
Family-based association studies for next-generation sequencing.
@ast
Family-based association studies for next-generation sequencing.
@en
P2860
P1476
Family-based association studies for next-generation sequencing
@en
P2093
Momiao Xiong
P2860
P304
P356
10.1016/J.AJHG.2012.04.022
P407
P50
P577
2012-06-01T00:00:00Z