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URL: http://theory.stanford.edu/~xuying/hapar/
Proper Citation: HAPAR (RRID:SCR_009218)
Description: Software application to infer haplotype from genotype data. It uses the parsimony principle, i.e. try to find the minimum number of haplotypes that can reconstruct the input genotypes. (entry from Genetic Analysis Software)
Abbreviations: HAPAR
Synonyms: HAplotype inference by PARsimony
Resource Type: software application, software resource
Keywords: gene, genetic, genomic, ms-window, unix, solaris
Resource Name: HAPAR
Resource ID: SCR_009218
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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