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Manage huge database

On Mon, 22 Sep 2008, Martin Morgan wrote:

            
<snip>>
netCDF is another useful option -- we have been using the ncdf package for 
large genomic datasets.  We read the data in one person at a time and 
write to netCDF.  For analysis we can then read any subsets.  Since we 
have imputed SNP data  as well as measured this comes to about 2.5 million 
variables on 4000 people for one of our data sets.


 	-thomas

Thomas Lumley			Assoc. Professor, Biostatistics
tlumley at u.washington.edu	University of Washington, Seattle