TOO SIMPLE. “Under the classical scheme, a mutation is compared to a wild-type reference, and its phenotypic effects are used to infer gene function. This framework often leads to a semantic shortcut: from a genetic change causing a variation in phenotype, it is often convenient to assimilate the corresponding gene as a causal determinant of a trait.”
https://lnkd.in/d3vzXnd
linkedin post 2022-06-29 05:12:48
Nigel Fleming
September 21, 2022