Thevalue means nothing on its own- it is used to find the probability that, assuming the hypothesis is true, the observed data set could have resulted from random fluctuations. A low probability suggests that the observed data are consistent with the hypothesis, and thus the hypothesis should be rejected, A standard cutoff point used by biologists is a probability of 0.05(5%). If the probability corresponding to thevalue is 0.05or considered statistically significant, the hypothesis (that the genes are unlinked) should be rejected. If the probability is above 0.05, the results are not statistically significant: the observed data are consistent with the hypothesis.
To find the probability, locate yourvalue in theDistribution table in Appendix F. The โdegree of freedomโ (pdf) of your data set is the number of categories (here,4 phenotypes), minus 1, so df=3.
(a). Determines which values on the df =3 line of the table your calculatedvalue lies between.
(b). The column headings for these values show the probability range for yournumber. Based on whether there is non-significant (p0.05) or significant (p>0.05) difference between the observed and expected values, are the data consistent with the hypothesis that the two genes are unlinked and assorting independently, or is there enough evidence to reject this hypothesis?