Experimentwise Error Rate
Contents |
may be challenged and removed. (June 2016) (Learn how and when to remove this template message) In statistics, family-wise
Experimentwise Error Definition
error rate (FWER) is the probability of making one or comparisonwise error rate more false discoveries, or type I errors, among all the hypotheses when performing multiple hypotheses familywise error rate tests. Contents 1 History 2 Background 2.1 Classification of multiple hypothesis tests 3 Definition 4 Controlling procedures 4.1 The Bonferroni procedure 4.2 The Šidák procedure
Comparison Wise Error Rate
4.3 Tukey's procedure 4.4 Holm's step-down procedure (1979) 4.5 Hochberg's step-up procedure 4.6 Dunnett's correction 4.7 Scheffé's method 4.8 Resampling procedures 5 Alternative approaches 6 References History[edit] Tukey coined the terms experimentwise error rate and "error rate per-experiment" to indicate error rates that the researcher could use as a control
Type 1 Error
level in a multiple hypothesis experiment.[citation needed] Background[edit] Within the statistical framework, there are several definitions for the term "family": Hochberg & Tamhane defined "family" in 1987 as "any collection of inferences for which it is meaningful to take into account some combined measure of error".[1][pageneeded] According to Cox in 1982, a set of inferences should be regarded a family:[citation needed] To take into account the selection effect due to data dredging To ensure simultaneous correctness of a set of inferences as to guarantee a correct overall decision To summarize, a family could best be defined by the potential selective inference that is being faced: A family is the smallest set of items of inference in an analysis, interchangeable about their meaning for the goal of research, from which selection of results for action, presentation or highlighting could be made (Yoav Benjamini).[citation needed] Classification of multiple hypothesis tests[edit] Main
Descriptive Statistics Hypothesis Testing General Properties of Distributions Distributions Normal Distribution Sampling Distributions Binomial and Related Distributions Student's t Distribution Chi-square and F Distributions Other Key Distributions Testing for Normality and Symmetry ANOVA One-way ANOVA Factorial ANOVA familywise error rate calculator ANOVA with Random or Nested Factors Design of Experiments ANOVA with Repeated Measures Analysis
Decision Wise Error Rate
of Covariance (ANCOVA) Miscellaneous Correlation Reliability Non-parametric Tests Time Series Analysis Survival Analysis Handling Missing Data Regression Linear Regression Multiple Regression per comparison error rate Logistic Regression Multinomial and Ordinal Logistic Regression Log-linear Regression Multivariate Descriptive Multivariate Statistics Multivariate Normal Distribution Hotelling’s T-square MANOVA Repeated Measures Tests Box’s Test Factor Analysis Cluster Analysis Appendix Mathematical Notation Excel Capabilities Matrices https://en.wikipedia.org/wiki/Family-wise_error_rate and Iterative Procedures Linear Algebra and Advanced Matrix Topics Other Mathematical Topics Statistics Tables Bibliography Author Citation Blogs Tools Real Statistics Functions Multivariate Functions Time Series Analysis Functions Missing Data Functions Data Analysis Tools Contact Us Experiment-wise error rate We could have conducted the analysis for Example 1 of Basic Concepts for ANOVA by conducting multiple two sample tests. E.g. to decide whether or not to reject the following null http://www.real-statistics.com/one-way-analysis-of-variance-anova/experiment-wise-error-rate/ hypothesis H0: μ1 = μ2 = μ3 We can use the following three separate null hypotheses: H0: μ1 = μ2 H0: μ2 = μ3 H0: μ1 = μ3 If any of these null hypotheses is rejected then the original null hypothesis is rejected. Note however that if you set α = .05 for each of the three sub-analyses then the overall alpha value is .14 since 1 – (1 – α)3 = 1 – (1 – .05)3 = 0.142525 (see Example 6 of Basic Probability Concepts). This means that the probability of rejecting the null hypothesis even when it is true (type I error) is 14.2525%. For k groups, you would need to run m = COMBIN(k, 2) such tests and so the resulting overall alpha would be 1 – (1 – α)m, a value which would get progressively higher as the number of samples increases. For example, if k = 6, then m = 15 and the probability of finding at least one significant t-test, purely by chance, even when the null hypothesis is true is over 50%. In fact, one of the reasons for performing ANOVA instead of separate t-tests is to reduce the type I error. The only problem is that once you have performed ANOVA if the null hypothesis is rejected you will naturally want to determine which
the simple question posed by an analysis of variance - do at least two treatment means differ? It may be that embedded in a group of treatments there is only one "control" treatment to which every other treatment should be compared, and comparisons among the non-control treatments may http://online.sfsu.edu/efc/classes/biol458/multcomp/multcomp.htm be uninteresting. One may also, after performing an analysis of variance and rejecting the null hypothesis of http://www.ncbi.nlm.nih.gov/pubmed/1184817 equality of treatment means want to know exactly which treatments or groups of treatments differ. To answer these kinds of questions requires careful consideration of the hypotheses of interest both before and after an experiment is conducted, the Type I error rate selected for each hypothesis, the power of each hypothesis test, and the Type I error rate acceptable for the group of hypotheses as a whole. error rate Comparisons or Contrasts If we let represent a treatment mean and ci a weight associated with the ith treatment mean then a comparison or contrast can be represented as: , where It can be seen that this contrast is a linear combination of treatment means (other contrasts such as quadratic and cubic are also possible). All of the following are possible comparisons: because they are weighted linear combinations of treatment means and the weights sum wise error rate to zero. For example, previously we have performed comparisons between two treatment means using the t - statistic: with (n1 + n2) - 2 degrees of freedom. This statistic is a "contrast." The numerator of this expression follows the general form of the contrast outlined above with the weights c1 and c2 equal to 1 and -1, respectively: However, we also see that this contrast is divided by the pooled within cell or within group variation. So, a contrast is actually the ratio of a linear combination of weighted means to an estimate of the pooled within cell or error variation in the experiment: with degrees of freedom. For a non - directional null hypothesis t could be replaced by F: with 1, and degrees of freedom. In general, a contrast is the ratio of a linear combination of weighted means to the mean square within cells times the sum of the squares of the weights assigned to each mean divided by the sample size within cells: where the cI' s are the weights assigned to each treatment mean,, ni is the number of observations in each cell and MSerror is the within cell variation pooled from the entire experiment (the within cell mean square estimated from a variance partition). For a comparison of two treatment means c1 = 1 and c2 = -1, so: n1+n2 -2 degrees of freedom, or with 1, and degrees of freedom. More genera
& Bioassays Resources...DNA & RNABLAST (Basic Local Alignment Search Tool)BLAST (Stand-alone)E-UtilitiesGenBankGenBank: BankItGenBank: SequinGenBank: tbl2asnGenome WorkbenchInfluenza VirusNucleotide DatabasePopSetPrimer-BLASTProSplignReference Sequence (RefSeq)RefSeqGeneSequence Read Archive (SRA)SplignTrace ArchiveUniGeneAll DNA & RNA Resources...Data & SoftwareBLAST (Basic Local Alignment Search Tool)BLAST (Stand-alone)Cn3DConserved Domain Search Service (CD Search)E-UtilitiesGenBank: BankItGenBank: SequinGenBank: tbl2asnGenome ProtMapGenome WorkbenchPrimer-BLASTProSplignPubChem Structure SearchSNP Submission ToolSplignVector Alignment Search Tool (VAST)All Data & Software Resources...Domains & StructuresBioSystemsCn3DConserved Domain Database (CDD)Conserved Domain Search Service (CD Search)Structure (Molecular Modeling Database)Vector Alignment Search Tool (VAST)All Domains & Structures Resources...Genes & ExpressionBioSystemsDatabase of Genotypes and Phenotypes (dbGaP)E-UtilitiesGeneGene Expression Omnibus (GEO) Database Gene Expression Omnibus (GEO) DatasetsGene Expression Omnibus (GEO) ProfilesGenome WorkbenchHomoloGeneMap ViewerOnline Mendelian Inheritance in Man (OMIM)RefSeqGeneUniGeneAll Genes & Expression Resources...Genetics & MedicineBookshelfDatabase of Genotypes and Phenotypes (dbGaP)Genetic Testing RegistryInfluenza VirusMap ViewerOnline Mendelian Inheritance in Man (OMIM)PubMedPubMed Central (PMC)PubMed Clinical QueriesRefSeqGeneAll Genetics & Medicine Resources...Genomes & MapsDatabase of Genomic Structural Variation (dbVar)GenBank: tbl2asnGenomeGenome ProjectGenome ProtMapGenome WorkbenchInfluenza VirusMap ViewerNucleotide DatabasePopSetProSplignSequence Read Archive (SRA)SplignTrace ArchiveAll Genomes & Maps Resources...HomologyBLAST (Basic Local Alignment Search Tool)BLAST (Stand-alone)BLAST Link (BLink)Conserved Domain Database (CDD)Conserved Domain Search Service (CD Search)Genome ProtMapHomoloGeneProtein ClustersAll Homology Resources...LiteratureBookshelfE-UtilitiesJournals in NCBI DatabasesMeSH DatabaseNCBI HandbookNCBI Help ManualNCBI NewsPubMedPubMed Central (PMC)PubMed Clinical QueriesPubMed HealthAll Literature Resources...ProteinsBioSystemsBLAST (Basic Local Alignment Search Tool)BLAST (Stand-alone)BLAST Link (BLink)Conserved Domain Database (CDD)Conserved Domain Search Service (CD Search)E-UtilitiesProSplignProtein ClustersProtein DatabaseReference Sequence (RefSeq)All Proteins Resources...Sequence AnalysisBLAST (Basic Local Alignment