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How do we translate variant information between human genome releases? #11

Open aneilbaboo opened 6 years ago

taltman commented 6 years ago

This can arise both from people curating information about pathogenic variants where the literature or database references a variant coordinate on an older human genome release, or when processing older genotyping data files from customers that report the variants relative to an older human genome release.

taltman commented 6 years ago

This will need to be addressed in a release after Release 1.