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URL: http://www.unc.edu/~yunmli/betaseq/
Proper Citation: BETASEQ (RRID:SCR_006401)
Description: Software to control Type-I error inflation in partially sequenced data for rare variant association testing. It is typically used to combine sequence and genotype data for the two stage design, in which individuals sequenced in stage one for variant detection are solely or predominantly cases then in stage two the discovered variants are genotyped in the remaining individuals. BETASEQ can work with any existing rare variant association methods that use genotypes or imputed genotypes as input.
Abbreviations: BETASEQ
Resource Type: software resource
Defining Citation: PMID:24336643
Keywords: variant association testing, variant association, variant
Availability: Free, Public
Resource Name: BETASEQ
Resource ID: SCR_006401
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University of North Carolina at Chapel Hill; North Carolina; USA |
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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
