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URL: https://atgu.mgh.harvard.edu/plinkseq/
Proper Citation: PLINK/SEQ (RRID:SCR_013193)
Description: An open-source C/C++ library for working with human genetic variation data. The specific focus is to provide a platform for analytic tool development for variation data from large-scale resequencing projects, particularly whole-exome and whole-genome studies. However, the library could in principle be applied to other types of genetic studies, including whole-genome association studies of common SNPs. (entry from Genetic Analysis Software)
Resource Type: software application, software library, software resource, software toolkit
Keywords: gene, genetic, genomic, c/c++, r, macos, linux, bio.tools
Availability: Open unspecified license
Resource Name: PLINK/SEQ
Resource ID: SCR_013193
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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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