GEMINI (GEnome MINIng) is designed to be a flexible framework for exploring genetic variation in the context of the wealth of genome annotations available for the human genome. By placing genetic variants, sample genotypes, and useful genome annotations into an integrated database framework, GEMINI provides a simple, flexible, yet very powerful system for exploring genetic variation for for disease and population genetics. Using the GEMINI framework begins by loading a VCF file into a database. Each variant is automatically annotated by comparing it to several genome annotations from source such as ENCODE tracks, UCSC tracks, OMIM, dbSNP, KEGG, and HPRD. All of this information is stored in portable SQLite database that allows one to explore and interpret both coding and non-coding variation using "off-the-shelf" tools or an enhanced SQL engine. https://github.com/arq5x/gemini |
hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/package_gemini_0_18_1
Repository package_zlib_1_2_8 revision 411985b46ae8 owned by iuc (prior install required) |
Name | Version | Type | |
---|---|---|---|
gemini | 0.18.1 | package | |
zlib | 1.2.8 | package |