Optimal experimental design and sample size for the statistical evaluation of data from somatic mutation and recombination tests (SMART) in Drosophila

In genetic toxicology it is important to know whether chemicals should be regarded as clearly hazardous or whether they can be considered sufficiently safe, which latter would be the case from the genotoxicologist's view if their genotoxic effects are nil or at least significantly below a prede...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Mutation Research 1995-04, Vol.334 (2), p.247-258
Hauptverfasser: Frei, Hansjörg, Würgler, Friedrich E.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 258
container_issue 2
container_start_page 247
container_title Mutation Research
container_volume 334
creator Frei, Hansjörg
Würgler, Friedrich E.
description In genetic toxicology it is important to know whether chemicals should be regarded as clearly hazardous or whether they can be considered sufficiently safe, which latter would be the case from the genotoxicologist's view if their genotoxic effects are nil or at least significantly below a predefined minimal effect level. A previously presented statistical decision procedure which allows one to make precisely this distinction is now extended to the question of how optimal experimental sample size can be determined in advance for genotoxicity experiments using the somatic mutation and recombination tests (SMART) of Drosophila. Optimally, the statistical tests should have high power to minimise the chance for statistically inconclusive results. Based on the normal test, the statistical principles are explained, and in an application to the wing spot assay, it is shown how the practitioner can proceed to optimise sample size to achieve numerically satisfactory conditions for statistical testing. The somatic genotoxicity assays of Drosophila are in principle based on somatic spots (mutant clones) that are recovered in variable numbers on individual flies. The underlying frequency distributions are expected to be of the Poisson type. However, some care seems indicated with respect to this latter assumption, because pooling of data over individuals, sexes, and experiments, for example, can (but need not) lead to data which are overdispersed, i.e, the data may show more variability than theoretically expected. It is an undesired effect of overdispersion that in comparisons of pooled totals it can lead to statistical testing which is too liberal, because overall it yields too many seemingly significant results. If individual variability considered alone is not contradiction with Poisson expectation, however, experimental planning can help to minimise the undesired effects of overdispersion on statistical testing of pooled totals. The rule for the practice is to avoid disproportionate sampling. It is recalled that for optimal power in statistical testing, it is preferable to use equal total numbers of flies in the control and treated series. Statistical tests which are based on Poisson expectations are too liberal if there is overdispersion in the data due to excess individual variability. In this case we propose to use the U test as a non-parametric two-sample test and to adjust the estimated optimal sample size according to (i) the overdispersion observed in a lar
doi_str_mv 10.1016/0165-1161(95)90018-7
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_16899083</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0165116195900187</els_id><sourcerecordid>16899083</sourcerecordid><originalsourceid>FETCH-LOGICAL-c388t-ee8c02a43fd7b56bb071dc84e6d6b5c252d8744e0b023f327db51da790ac5fbe3</originalsourceid><addsrcrecordid>eNp9Uc1O3jAQ9KEVpbRv0Eo-ITiktZM4di6VEC0UCYQE9Gz5Z1OM4ji1HUT7IH1enOYTxx4sa2d2xutZhD5Q8okS2n0uh1WUdvSoZ8c9IVRU_BXaf4HfoLcpPRDSdqwWe2iPC8Ea3u-jv9dzdl6NGJ5miM7DlEthIbmfE1aTxUn5eQSc3B_AQ4g435ciq-xSdmbVPapxKWWYcBiwVVnhIQaPU_AFNdgveWNXswgmeO2mDcmQcsJHt1cnN3fH2E34awwpzPduVO_Q60GNCd7v7gP04-zb3en36vL6_OL05LIyjRC5AhCG1KptBss167QmnFojWuhsp5mpWW0Fb1sgmtTN0NTcakat4j1Rhg0amgN0uPnOMfxayjzSu2RgHNUEYUmSdqLviWhKY7s1mjJjijDIuaSl4m9JiVxXINes5Zq17Jn8twLJi-zjzn_RHuyLaJd_4b9sPJRPPjqIMhkHkwHrSlZZ2uD-_8AzOkibHQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16899083</pqid></control><display><type>article</type><title>Optimal experimental design and sample size for the statistical evaluation of data from somatic mutation and recombination tests (SMART) in Drosophila</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Frei, Hansjörg ; Würgler, Friedrich E.</creator><creatorcontrib>Frei, Hansjörg ; Würgler, Friedrich E.</creatorcontrib><description>In genetic toxicology it is important to know whether chemicals should be regarded as clearly hazardous or whether they can be considered sufficiently safe, which latter would be the case from the genotoxicologist's view if their genotoxic effects are nil or at least significantly below a predefined minimal effect level. A previously presented statistical decision procedure which allows one to make precisely this distinction is now extended to the question of how optimal experimental sample size can be determined in advance for genotoxicity experiments using the somatic mutation and recombination tests (SMART) of Drosophila. Optimally, the statistical tests should have high power to minimise the chance for statistically inconclusive results. Based on the normal test, the statistical principles are explained, and in an application to the wing spot assay, it is shown how the practitioner can proceed to optimise sample size to achieve numerically satisfactory conditions for statistical testing. The somatic genotoxicity assays of Drosophila are in principle based on somatic spots (mutant clones) that are recovered in variable numbers on individual flies. The underlying frequency distributions are expected to be of the Poisson type. However, some care seems indicated with respect to this latter assumption, because pooling of data over individuals, sexes, and experiments, for example, can (but need not) lead to data which are overdispersed, i.e, the data may show more variability than theoretically expected. It is an undesired effect of overdispersion that in comparisons of pooled totals it can lead to statistical testing which is too liberal, because overall it yields too many seemingly significant results. If individual variability considered alone is not contradiction with Poisson expectation, however, experimental planning can help to minimise the undesired effects of overdispersion on statistical testing of pooled totals. The rule for the practice is to avoid disproportionate sampling. It is recalled that for optimal power in statistical testing, it is preferable to use equal total numbers of flies in the control and treated series. Statistical tests which are based on Poisson expectations are too liberal if there is overdispersion in the data due to excess individual variability. In this case we propose to use the U test as a non-parametric two-sample test and to adjust the estimated optimal sample size according to (i) the overdispersion observed in a large historical control and (ii) the relative efficiency of the U test in comparison to the t test and related parametric tests.</description><identifier>ISSN: 0165-1161</identifier><identifier>ISSN: 0027-5107</identifier><identifier>DOI: 10.1016/0165-1161(95)90018-7</identifier><identifier>PMID: 7885379</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Chi-Square Distribution ; Drosophila ; Drosophila melanogaster ; Drosophila melanogaster - drug effects ; Drosophila melanogaster - genetics ; Experimental design ; Eye Color - genetics ; Female ; Genetic Variation ; Male ; Maximum Allowable Concentration ; Models, Genetic ; Models, Statistical ; Mutagenicity Tests - methods ; Mutagenicity Tests - statistics &amp; numerical data ; Mutagens - toxicity ; Mutation ; Overdispersion ; Poisson Distribution ; Poisson expectation ; Recombination, Genetic ; Reproducibility of Results ; Sample Size ; Somatic genotoxicity tests (SMART) ; Statistics ; Statistics, Nonparametric ; Wings, Animal - abnormalities</subject><ispartof>Mutation Research, 1995-04, Vol.334 (2), p.247-258</ispartof><rights>1995</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c388t-ee8c02a43fd7b56bb071dc84e6d6b5c252d8744e0b023f327db51da790ac5fbe3</citedby><cites>FETCH-LOGICAL-c388t-ee8c02a43fd7b56bb071dc84e6d6b5c252d8744e0b023f327db51da790ac5fbe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7885379$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frei, Hansjörg</creatorcontrib><creatorcontrib>Würgler, Friedrich E.</creatorcontrib><title>Optimal experimental design and sample size for the statistical evaluation of data from somatic mutation and recombination tests (SMART) in Drosophila</title><title>Mutation Research</title><addtitle>Mutat Res</addtitle><description>In genetic toxicology it is important to know whether chemicals should be regarded as clearly hazardous or whether they can be considered sufficiently safe, which latter would be the case from the genotoxicologist's view if their genotoxic effects are nil or at least significantly below a predefined minimal effect level. A previously presented statistical decision procedure which allows one to make precisely this distinction is now extended to the question of how optimal experimental sample size can be determined in advance for genotoxicity experiments using the somatic mutation and recombination tests (SMART) of Drosophila. Optimally, the statistical tests should have high power to minimise the chance for statistically inconclusive results. Based on the normal test, the statistical principles are explained, and in an application to the wing spot assay, it is shown how the practitioner can proceed to optimise sample size to achieve numerically satisfactory conditions for statistical testing. The somatic genotoxicity assays of Drosophila are in principle based on somatic spots (mutant clones) that are recovered in variable numbers on individual flies. The underlying frequency distributions are expected to be of the Poisson type. However, some care seems indicated with respect to this latter assumption, because pooling of data over individuals, sexes, and experiments, for example, can (but need not) lead to data which are overdispersed, i.e, the data may show more variability than theoretically expected. It is an undesired effect of overdispersion that in comparisons of pooled totals it can lead to statistical testing which is too liberal, because overall it yields too many seemingly significant results. If individual variability considered alone is not contradiction with Poisson expectation, however, experimental planning can help to minimise the undesired effects of overdispersion on statistical testing of pooled totals. The rule for the practice is to avoid disproportionate sampling. It is recalled that for optimal power in statistical testing, it is preferable to use equal total numbers of flies in the control and treated series. Statistical tests which are based on Poisson expectations are too liberal if there is overdispersion in the data due to excess individual variability. In this case we propose to use the U test as a non-parametric two-sample test and to adjust the estimated optimal sample size according to (i) the overdispersion observed in a large historical control and (ii) the relative efficiency of the U test in comparison to the t test and related parametric tests.</description><subject>Animals</subject><subject>Chi-Square Distribution</subject><subject>Drosophila</subject><subject>Drosophila melanogaster</subject><subject>Drosophila melanogaster - drug effects</subject><subject>Drosophila melanogaster - genetics</subject><subject>Experimental design</subject><subject>Eye Color - genetics</subject><subject>Female</subject><subject>Genetic Variation</subject><subject>Male</subject><subject>Maximum Allowable Concentration</subject><subject>Models, Genetic</subject><subject>Models, Statistical</subject><subject>Mutagenicity Tests - methods</subject><subject>Mutagenicity Tests - statistics &amp; numerical data</subject><subject>Mutagens - toxicity</subject><subject>Mutation</subject><subject>Overdispersion</subject><subject>Poisson Distribution</subject><subject>Poisson expectation</subject><subject>Recombination, Genetic</subject><subject>Reproducibility of Results</subject><subject>Sample Size</subject><subject>Somatic genotoxicity tests (SMART)</subject><subject>Statistics</subject><subject>Statistics, Nonparametric</subject><subject>Wings, Animal - abnormalities</subject><issn>0165-1161</issn><issn>0027-5107</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uc1O3jAQ9KEVpbRv0Eo-ITiktZM4di6VEC0UCYQE9Gz5Z1OM4ji1HUT7IH1enOYTxx4sa2d2xutZhD5Q8okS2n0uh1WUdvSoZ8c9IVRU_BXaf4HfoLcpPRDSdqwWe2iPC8Ea3u-jv9dzdl6NGJ5miM7DlEthIbmfE1aTxUn5eQSc3B_AQ4g435ciq-xSdmbVPapxKWWYcBiwVVnhIQaPU_AFNdgveWNXswgmeO2mDcmQcsJHt1cnN3fH2E34awwpzPduVO_Q60GNCd7v7gP04-zb3en36vL6_OL05LIyjRC5AhCG1KptBss167QmnFojWuhsp5mpWW0Fb1sgmtTN0NTcakat4j1Rhg0amgN0uPnOMfxayjzSu2RgHNUEYUmSdqLviWhKY7s1mjJjijDIuaSl4m9JiVxXINes5Zq17Jn8twLJi-zjzn_RHuyLaJd_4b9sPJRPPjqIMhkHkwHrSlZZ2uD-_8AzOkibHQ</recordid><startdate>19950401</startdate><enddate>19950401</enddate><creator>Frei, Hansjörg</creator><creator>Würgler, Friedrich E.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19950401</creationdate><title>Optimal experimental design and sample size for the statistical evaluation of data from somatic mutation and recombination tests (SMART) in Drosophila</title><author>Frei, Hansjörg ; Würgler, Friedrich E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c388t-ee8c02a43fd7b56bb071dc84e6d6b5c252d8744e0b023f327db51da790ac5fbe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Chi-Square Distribution</topic><topic>Drosophila</topic><topic>Drosophila melanogaster</topic><topic>Drosophila melanogaster - drug effects</topic><topic>Drosophila melanogaster - genetics</topic><topic>Experimental design</topic><topic>Eye Color - genetics</topic><topic>Female</topic><topic>Genetic Variation</topic><topic>Male</topic><topic>Maximum Allowable Concentration</topic><topic>Models, Genetic</topic><topic>Models, Statistical</topic><topic>Mutagenicity Tests - methods</topic><topic>Mutagenicity Tests - statistics &amp; numerical data</topic><topic>Mutagens - toxicity</topic><topic>Mutation</topic><topic>Overdispersion</topic><topic>Poisson Distribution</topic><topic>Poisson expectation</topic><topic>Recombination, Genetic</topic><topic>Reproducibility of Results</topic><topic>Sample Size</topic><topic>Somatic genotoxicity tests (SMART)</topic><topic>Statistics</topic><topic>Statistics, Nonparametric</topic><topic>Wings, Animal - abnormalities</topic><toplevel>online_resources</toplevel><creatorcontrib>Frei, Hansjörg</creatorcontrib><creatorcontrib>Würgler, Friedrich E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Mutation Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frei, Hansjörg</au><au>Würgler, Friedrich E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimal experimental design and sample size for the statistical evaluation of data from somatic mutation and recombination tests (SMART) in Drosophila</atitle><jtitle>Mutation Research</jtitle><addtitle>Mutat Res</addtitle><date>1995-04-01</date><risdate>1995</risdate><volume>334</volume><issue>2</issue><spage>247</spage><epage>258</epage><pages>247-258</pages><issn>0165-1161</issn><issn>0027-5107</issn><abstract>In genetic toxicology it is important to know whether chemicals should be regarded as clearly hazardous or whether they can be considered sufficiently safe, which latter would be the case from the genotoxicologist's view if their genotoxic effects are nil or at least significantly below a predefined minimal effect level. A previously presented statistical decision procedure which allows one to make precisely this distinction is now extended to the question of how optimal experimental sample size can be determined in advance for genotoxicity experiments using the somatic mutation and recombination tests (SMART) of Drosophila. Optimally, the statistical tests should have high power to minimise the chance for statistically inconclusive results. Based on the normal test, the statistical principles are explained, and in an application to the wing spot assay, it is shown how the practitioner can proceed to optimise sample size to achieve numerically satisfactory conditions for statistical testing. The somatic genotoxicity assays of Drosophila are in principle based on somatic spots (mutant clones) that are recovered in variable numbers on individual flies. The underlying frequency distributions are expected to be of the Poisson type. However, some care seems indicated with respect to this latter assumption, because pooling of data over individuals, sexes, and experiments, for example, can (but need not) lead to data which are overdispersed, i.e, the data may show more variability than theoretically expected. It is an undesired effect of overdispersion that in comparisons of pooled totals it can lead to statistical testing which is too liberal, because overall it yields too many seemingly significant results. If individual variability considered alone is not contradiction with Poisson expectation, however, experimental planning can help to minimise the undesired effects of overdispersion on statistical testing of pooled totals. The rule for the practice is to avoid disproportionate sampling. It is recalled that for optimal power in statistical testing, it is preferable to use equal total numbers of flies in the control and treated series. Statistical tests which are based on Poisson expectations are too liberal if there is overdispersion in the data due to excess individual variability. In this case we propose to use the U test as a non-parametric two-sample test and to adjust the estimated optimal sample size according to (i) the overdispersion observed in a large historical control and (ii) the relative efficiency of the U test in comparison to the t test and related parametric tests.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>7885379</pmid><doi>10.1016/0165-1161(95)90018-7</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0165-1161
ispartof Mutation Research, 1995-04, Vol.334 (2), p.247-258
issn 0165-1161
0027-5107
language eng
recordid cdi_proquest_miscellaneous_16899083
source MEDLINE; Alma/SFX Local Collection
subjects Animals
Chi-Square Distribution
Drosophila
Drosophila melanogaster
Drosophila melanogaster - drug effects
Drosophila melanogaster - genetics
Experimental design
Eye Color - genetics
Female
Genetic Variation
Male
Maximum Allowable Concentration
Models, Genetic
Models, Statistical
Mutagenicity Tests - methods
Mutagenicity Tests - statistics & numerical data
Mutagens - toxicity
Mutation
Overdispersion
Poisson Distribution
Poisson expectation
Recombination, Genetic
Reproducibility of Results
Sample Size
Somatic genotoxicity tests (SMART)
Statistics
Statistics, Nonparametric
Wings, Animal - abnormalities
title Optimal experimental design and sample size for the statistical evaluation of data from somatic mutation and recombination tests (SMART) in Drosophila
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T04%3A04%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Optimal%20experimental%20design%20and%20sample%20size%20for%20the%20statistical%20evaluation%20of%20data%20from%20somatic%20mutation%20and%20recombination%20tests%20(SMART)%20in%20Drosophila&rft.jtitle=Mutation%20Research&rft.au=Frei,%20Hansj%C3%B6rg&rft.date=1995-04-01&rft.volume=334&rft.issue=2&rft.spage=247&rft.epage=258&rft.pages=247-258&rft.issn=0165-1161&rft_id=info:doi/10.1016/0165-1161(95)90018-7&rft_dat=%3Cproquest_cross%3E16899083%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16899083&rft_id=info:pmid/7885379&rft_els_id=0165116195900187&rfr_iscdi=true