Difference between revisions of "KING"
Jump to navigation
Jump to search
Moskalenko (talk | contribs) (Created page with "Category:SoftwareCategory:BioinformaticsCategory:Genomics {|<!--CONFIGURATION: REQUIRED--> |{{#vardefine:app|king}} |{{#vardefine:url|http://people.virginia.edu/~w...") |
|||
Line 70: | Line 70: | ||
<!--Turn the Table of Contents and Edit paragraph links ON/OFF--> | <!--Turn the Table of Contents and Edit paragraph links ON/OFF--> | ||
__NOTOC____NOEDITSECTION__ | __NOTOC____NOEDITSECTION__ | ||
+ | =Validation= | ||
+ | * Validated 4/5/2018 |
Revision as of 19:21, 5 April 2018
Description
KING is a toolset making use of high-throughput SNP data typically seen in a genome-wide association study (GWAS) or a sequencing project. Applications of KING include family relationship inference and pedigree error checking, population substructure identification, forensics, gene mapping, etc.
Software Manual in HTML format
Required Modules
Serial
- king
System Variables
- HPC_{{#uppercase:king}}_DIR
Citation
If you publish research that uses king you have to cite it as follows:
Manichaikul A, Mychaleckyj JC, Rich SS, Daly K, Sale M, Chen WM (2010) Robust relationship inference in genome-wide association studies. Bioinformatics 26(22):2867-2873
Validation
- Validated 4/5/2018