You can sequence for genotypes, and do selection based on the results of genomic studies.
I read this and all I can think of is the recent family 23andme results with half-opposite results of what they 'should' be for risk factors given known family history back three generations indicating that whatever is causing the risk is completely unknown to genetic science, and a recent study in which only 15% of the genetic basis for height (known to be >80% responsible) was discovered spread over more than 400 loci... don't get me wrong there's hardly any reason anybody should be conceived with simple common mendelian diseases these days, but if you wanted to actually change much other than that or gross differences in brain or liver chemistry you need to actually observe phenotype.
The article by Robert Sparrow:
Quote:
The possibility was discussed in MIRI's "Uncertain Future" toy forecasting model back in 2009, and the analysis formulated a few years before that.
ETA: And further discussed in James Miller's recent book, "Singularity Rising."