FastNgsAdmixOld: Difference between revisions
Jump to navigation
Jump to search
Kehanghoej (talk | contribs) No edit summary |
Kehanghoej (talk | contribs) No edit summary |
||
Line 11: | Line 11: | ||
=Run example= | =Run example= | ||
First download some example test files which has been generated on basis of data from the 1000 genomes project. | |||
<pre> | |||
wget popgen.dk/??????/popfreq.RData | |||
wget popgen.dk/?????? | |||
</pre> | |||
<pre> | |||
HOME$ Rscript NGS_Admix_rscript.r beagle_GL='indi_genotypelikelihood.beagle' popfreq_RDATA='pop_freq_all.RData' outputfile='test' | |||
</pre> | |||
=Input Files= | =Input Files= |
Revision as of 20:17, 21 September 2014
This page contains information about the program called FastNGSadmix, which is a very fast tool for finding admixture proportions from NGS data of a single individual. It is based on genotype likelihoods. The program is written in R.
Installation
wget popgen.dk/?? OR Use shiny: popgen.dk/???
Run example
First download some example test files which has been generated on basis of data from the 1000 genomes project.
wget popgen.dk/??????/popfreq.RData wget popgen.dk/??????
HOME$ Rscript NGS_Admix_rscript.r beagle_GL='indi_genotypelikelihood.beagle' popfreq_RDATA='pop_freq_all.RData' outputfile='test'