Abstract
AbstractA method is devised for determining the statistical significance of the difference between a mutation frequency observed after treatment with a potential mutagen and its control frequency. This procedure, however, can be used only when the respective control value is based on large and reliable material (“stable” controls), a requirement that seems to be met in at least part of the systems used for mutagenesis screening. The procedure proposed has some advantages when compared with the 2 and the KASTENBAUM‐BOWMAN test, the most important one being that it can be employed when these two tests cannot (because of expected frequencies <5 in the 2 test and limited tabulations of the N and p values in the KASTENBAUM‐BOWMAN test). After explaining the procedure, an instruction how to carry it out is presented and illustrated by two examples (recessive sex‐linked lethal mutations in Drosophila melanogaster and dicentric chromosomes in human lymphocytes).
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.