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URL: http://cran.r-project.org/web/packages/CNVassoc/
Proper Citation: CNVassoc (RRID:SCR_002901)
Description: Software package that carries out association analysis of common copy number variants in population-based studies. It includes functions for analysing association under a series of study designs (case-control, cohort, etc), using several dependent variables (class status, censored data, counts) as response, adjusting for covariates and considering various inheritance models. It also includes functions for inferring copy number (CNV genotype calling). Various classes and methods for generic functions (print, summary, plot, anova, ... ) have been created to facilitate the analysis.
Synonyms: CNVassoc: Association analysis of CNV data
Resource Type: software resource
Defining Citation: PMID:21609482
Keywords: standalone software, mac os x, unix/linux, windows, r
Availability: THIS RESOURCE IS NO LONGER IN SERVICE
Resource Name: CNVassoc
Resource ID: SCR_002901
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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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