Evaluating methods for combining rare variant data in pathway-based tests of genetic association

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Evaluating methods for combining rare variant data in pathway-based tests of genetic association is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1007618551
P356DOI10.1186/1753-6561-5-S9-S48
P932PMC publication ID3287885
P698PubMed publication ID22373429

P2093author name stringScott Powers
Nathan L Tintle
Ashley Petersen
Alexandra Sitarik
Alexander Luedtke
Airat Bekmetjev
P2860cites workGene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profilesQ24536351
Inclusion of a priori information in genome-wide association analysisQ28749654
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence dataQ33359015
A groupwise association test for rare mutations using a weighted sum statisticQ33408787
Comparing gene set analysis methods on single-nucleotide polymorphism data from Genetic Analysis Workshop 16.Q33519414
Evaluating methods for the analysis of rare variants in sequence dataQ34176920
Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypesQ34300842
Powerful SNP-set analysis for case-control genome-wide association studiesQ34544433
Pathway-based approaches for analysis of genomewide association studiesQ36512103
An evaluation of statistical approaches to rare variant analysis in genetic association studiesQ39941009
On the utility of gene set methods in genomewide association studies of quantitative traitsQ45424372
P275copyright licenseCreative Commons Attribution 2.0 GenericQ19125117
P6216copyright statuscopyrightedQ50423863
P304page(s)S48
P577publication date2011-11-29
P1433published inBMC ProceedingsQ27721520
P1476titleEvaluating methods for combining rare variant data in pathway-based tests of genetic association
P478volume5 Suppl 9

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cites work (P2860)
Q34085512Application of family-based tests of association for rare variants to pathways
Q34614279Assessing the impact of differential genotyping errors on rare variant tests of association
Q34086434Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17.
Q42977183Pathway analysis approaches for rare and common variants: insights from Genetic Analysis Workshop 18.
Q30834583Pathway analysis with next-generation sequencing data
Q38992286The road to precision psychiatry: translating genetics into disease mechanisms.

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