KATE
A program that analyses the effects of low frequency and rare variants on quantitative traits within a chromosomal region
About
Single-point analysis of low-frequency and rare variants is under-powered, as not enough copies of the minor allele are observed. An alternative approach is to use methods that combine information across multiple low frequency or rare variant sites within a region. Focusing on the analysis of quantitative traits, we developed KATE (Kernel Association Test Extended) that uses the Allele Match kernel to cluster individuals into disjoint clusters and tests the cluster-specific effects via ANOVA.
Downloads
System requirements
The software should run on any UNIX or GNU/Linux system.
Download KATE
After downloading the files, please read the KATE_README.txt file to set up and run the file.
Contact
If you need help or have any queries, please contact us using the details below.
If you have any problems running KATE, then please contact either Ioanna Tachmazidou or Eleftheria Zeggini.
It is recommended that you contact the author of KATE, Ioanna Tachmazidou regarding bugs or problems running the script.
Sanger Institute Contributors
Previous contributors
Dr Ioanna Tachmazidou
Staff Scientist
Eleftheria Zeggini
Former Group Leader