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by pedrobeltrao 5188 days ago
Unfortunately, as far as I know there is very little useful phenotypic data along with these genomes to work with. I would rather have fewer genome sequences with better phenotypic information. Even with just 35 genome sequences of "individual" yeast genomes I could do a lot more interesting analysis because they are well studied in turns of phenotypes.
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The point is to look at genomic variations across the entirety of the human genome, not so much to match genomic variation to phenotype. What you're saying makes sense, but I think that is more a next step.