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URL: http://www.sanger.ac.uk/resources/software/ariel/
Proper Citation: ARIEL (RRID:SCR_009126)
Description: Software application that explores the effects of rare variants within complex traits through locus-based analysis. 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, ARIEL has been developed as a locus-wide regression-based collapsing approach that incorporates variant quality scores. (entry from Genetic Analysis Software)
Abbreviations: ARIEL
Synonyms: Accumulation of Rare variants Integrated and Extended Locus-specific test
Resource Type: software application, software resource
Keywords: gene, genetic, genomic, r, unix, linux
Resource Name: ARIEL
Resource ID: SCR_009126
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
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