The RRID (SCR_021271) is not the primary RRID. It is an alternate RRID or alternate ID.
URL: http://www.nitrc.org/projects/plink
Proper Citation: PLINK (RRID:SCR_001757)
Description: Open source whole genome association analysis toolset, designed to perform range of basic, large scale analyses in computationally efficient manner. Used for analysis of genotype/phenotype data. Through integration with gPLINK and Haploview, there is some support for subsequent visualization, annotation and storage of results. PLINK 1.9 is improved and second generation of the software.
Synonyms: PLINK 1.9, PLINK/SEQ, plink - Whole genome association analysis toolset
Resource Type: software resource, software application, software toolkit, data analysis software, data processing software
Defining Citation: PMID:17701901, DOI:10.1086/519795
Keywords: gene, genetic, genomic, genotype, phenotype, copy number variant, whole-genome association, population, linkage analysis, whole-genome association study, data management, summary statistics, population stratification, association analysis, identity-by-descent estimation
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Warning: PCA results may be sensitive to the sample size, population composition, and the number of columns, in which case the results will not be reliable, robust, nor replicable and should not be used to draw conclusions.
Source: SciCrunch Registry
