Designed for analysis of the results of a Genome Wide Association Study. Includes tools to pull lists of Chromosome number and SNP position below a certain significance threshold, refine gene networks (including data I/O for Cytoscape), and check SNP base pair changes.
|Maintainer||Angela Fan <firstname.lastname@example.org>|
|License||Artistic License 2.0|
|Package repository||View on CRAN|
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