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News
In development: a tool for scoring CNVs and runs of homozygosity using linkage results.
homruns: Version 0.1.2 fixes a number of path issues that prevented homruns from working on Windows systems.
homruns: Version 0.1.1 has been released, replacing 0.1 and fixing some chromosome index bugs that crashed homruns. Downloading the new version is highly recommended.
This is the website for homruns, a simple GUI application for searching SNP datasets for runs of homozygosity and Mendelian errors and visualizing the results.
Usage
Binary pedigree files (Plink bed + bim + fam format) should be used as input. The parameters that can be adjusted in the program have the same names as those for command-line use of Plink"s --homozyg mode. For details of what each of them do, see the Plin
