random phenotypic variation of yeast (saccharomyces cerevisiae) single-gene knockouts fits a double pareto-lognormal distribution随机的表型变异的酵母(酿酒酵母)单基因淘汰赛中适合双pareto-lognormal分布.pdfVIP
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random phenotypic variation of yeast (saccharomyces cerevisiae) single-gene knockouts fits a double pareto-lognormal distribution随机的表型变异的酵母(酿酒酵母)单基因淘汰赛中适合双pareto-lognormal分布
Random Phenotypic Variation of Yeast (Saccharomyces
cerevisiae) Single-Gene Knockouts Fits a Double Pareto-
Lognormal Distribution
1 2,3 1,4
John H. Graham *, Daniel T. Robb , Amy R. Poe
1 Department of Biology, Berry College, Mount Berry, Georgia, United States of America, 2 Department of Physics, Astronomy, and Geology, Berry College, Mount Berry,
Georgia, United States of America, 3 Department of Mathematics, Computer Science and Physics, Roanoke College, Salem, Virginia, United States of America, 4 Center for
Integrative Genomics, Georgia Institute of Technology, Atlanta, Georgia, United States of America
Abstract
Background: Distributed robustness is thought to influence the buffering of random phenotypic variation through the
scale-free topology of gene regulatory, metabolic, and protein-protein interaction networks. If this hypothesis is true, then
the phenotypic response to the perturbation of particular nodes in such a network should be proportional to the number of
links those nodes make with neighboring nodes. This suggests a probability distribution approximating an inverse power-
law of random phenotypic variation. Zero phenotypic variation, however, is impossible, because random molecular and
cellular processes are essential to normal development. Consequently, a more realistic distribution should have a y-intercept
close to zero in the lower tail, a mode greater than zero, and a long (fat) upper tail. The double Pareto-lognormal (DPLN)
distribution is an ideal candidate distribution. It consists of a mixture of a lognormal body and upper and lower power-law
tails.
Objective and Methods: If our assumptions are true, the DPLN distribution should provide a better fit to random
phenotypic variation in a large series
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