Post date: Aug 23, 2013 5:30:34 PM
I parsed the low frequency and rare variant data sets down to 15,076 SNVs (the first 15,076 in each file) to make them comparable to the common variant data and to reduce the time needed for MCMC. I then submitted these jobs to the research computing cluster with the same options as the common variants (submitted earlier today, see the last post). These have job ids 5751-5778.