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Resource Name
AMELIA
RRID:SCR_009119 RRID Copied      
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AMELIA (RRID:SCR_009119)
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Resource Information

URL: http://www.sanger.ac.uk/resources/software/amelia/

Proper Citation: AMELIA (RRID:SCR_009119)

Description: Software application that employs allele matching to analyse the effects of rare variants within a specific locus. There is increasing evidence that rare variants play a role in some complex traits, but their analysis is not straightforward. Locus-based tests become necessary due to low power in rare variant single-point association analyses. In addition, variant quality scores are available for sequencing data, but are rarely taken into account. To enable this analysis, AMELIA has been developed as an allele-matching approach that is robust to the presence of both directions of effect for variants within the locus analysed. (entry from Genetic Analysis Software)

Abbreviations: AMELIA

Synonyms: Allele Matching Empirical Locus-specific Integrated Association test

Resource Type: software resource, software application

Keywords: gene, genetic, genomic, r, unix, linux

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