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Resource Name
RRID:SCR_001757 RRID Copied      
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PLINK (RRID:SCR_001757)
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Resource Information

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 application, data analysis software, software resource, 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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This resource

is listed by

OMICtools

is listed by

Genetic Analysis Software

is listed by

NeuroImaging Tools and Resources Collaboratory (NITRC)

is listed by

Debian

is listed by

SoftCite

is related to

Whap

is related to

PLINK/SEQ

is related to

Haploview

is related to

MendelIHT.jl

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