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NGS
,→Solutions
==Solutions==
[[PGx in Estonia|Solutions A solution for PGx on NGS genotyping biobank data]] are given has been investigated by ''Reisberg et al.'' in their article [https://doi.org/10.1101/356204 Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions]. An excellent solution for genotyping a collection of ADME (absorption, distribution, metabolism and elimination) genes for individual patients is Aldy, which is fast, accurate and relatively simple to use.
==Interesting publications==