Family-wise Error Rate Control in QTL Mapping and Gene Ontology Graphs

Size: px
Start display at page:

Download "Family-wise Error Rate Control in QTL Mapping and Gene Ontology Graphs"

Transcription

1 Family-wise Error Rate Control in QTL Mapping and Gene Ontology Graphs with Remarks on Family Selection Dissertation Defense April 5, 204

2 Contents Dissertation Defense Introduction 2 FWER Control within Gene Ontology Graphs 3 A Power Improving Multiplicity Correction for Large-Scale SNP Selection in LD Based QTL Mapping 4 QTL Mapping: Hypotheses and Approaches 5 Discussion

3 . Introduction Dissertation Defense If enough statistics are computed, some of them will be sure to show structure. (Diaconis 985).0 P(any type I error) Number of Simultaneous Tests (m)

4 . Introduction Dissertation Defense Cournot Tippet Great spurt of MCP activity Miller Marcus et al Hochberg & Tamhane Hsu Westfall & Young Denotes a world-wide conference on MCPs 's & 50's '87 '93 Number of MCP articles from four leading journals by year from 965 to '96 '00 '3

5 . Introduction Dissertation Defense The Vitality of [the] field in the future as a research area depends upon [the researcher s] ability to continue and address the real needs of statistical analysis in current problems (Benjamini, 200).

6 . Introduction Dissertation Defense Declared Declared non-significant significant Total True null hypothesis U V m 0 False null hypothesis T S m m 0 m R R m The Per Comparison Error Rate (PCER): E(V/m) The Familywise Error Rate (FWER): P(V ) The False Discovery Rate (FDR): E(V/R)

7 . Introduction Dissertation Defense Selecting a Family of Hypotheses A subjective, but important decision. Any collection of inferences for which it is meaningful to take into account some combined measure of errors. (Hochberg & Tamhane 987) Gatekeeping (Bretz et al. 2009)

8 . Introduction Dissertation Defense The Bonferroni Adjustment: test each H i at level α/m Boole s Inequality: P(A B) P(A)+P(B)... or generally P ( A i ) P(A i ) Let R i denote the event that hypothesis H i is rejected. Then, if P Hi (R i ) = α i, FWER = P Hi ( R i ) P Hi (R i ) = If α i = α/m for all i, then FWER α. α i

9 . Introduction Dissertation Defense Weighted Bonferroni Adjustment: test H i at level α i, s.t. α i α Since ( ) FWER = P Hi R i P Hi (R i ) = α i So long as α i α, then FWER α.

10 . Introduction Dissertation Defense Holm s Sequential Bonferroni: test ordered H (j) at level α/(m j + ) Let P i denoted the p-value for H i. Let I {,..., m} index the true H i, I = k m. Then, P (P i > α ) k for all i I = P (P i α ) k for some i I Since m j + k, FWER α. i I ( P P i α ) k k α k = α.

11 . Introduction Dissertation Defense Closed Testing: reject w i iff all w j w i are rejected at level α Let W be a set of hypotheses. W is closed under intersection if: for any two hypotheses H i, H j W, w = H i H j is also in W. An example Consider the elementary hypotheses H, H 2, and H 3. Let w = H, w 2 = H 2, w 3 = H 3, and w 4 = H H 2, w 5 = H H 3, w 6 = H 2 H 3, and w 7 = H H 2 H 3 W = {w,..., w 7 } is a set of hypotheses closed under intersections.

12 . Introduction Dissertation Defense Closed Testing: reject w i iff all w j w i are rejected at level α W = {w,..., w 7 } is a set of hypotheses closed under intersections. H H 2 H 3 w 7 H H 2 H 2 H 3 w 4 w 5 H H3 w 6 w w 2 w 3 H H 2 H 3

13 . Introduction Dissertation Defense Generalized Weighted Bonferroni Testing /2 α/3 /2 α/3 /2 α/3 H H 2 H 3 /2 /2 /2 mi= α i α 0 g ij, g ii = 0, and m k= g ik for all i, j =,..., m.

14 . Introduction Dissertation Defense Generalized Weighted Bonferroni Testing (a) α/2 α/2 (b) α H 2 H 3 H 3 mi= α i α 0 g ij, g ii = 0, and m k= g ik for all i, j =,..., m.

15 Contents Dissertation Defense Introduction 2 FWER Control within Gene Ontology Graphs 3 A Power Improving Multiplicity Correction for Large-Scale SNP Selection in LD Based QTL Mapping 4 QTL Mapping: Hypotheses and Approaches 5 Discussion

16 2. FWER Control within GO Graphs GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO:00530

17 2. FWER Control within GO Graphs (Toy) Example GO Graph A B F C D E

18 2. FWER Control within GO Graphs Focus Level Method (Goeman and Mansmann 2008) Applies a top-down and a bottom-up approach. (a) A (b) A (c) B F B F C E B CDE D CD DE CE CDE A BF CF CDF DF C D E CD DE CE F C D E

19 2. FWER Control within GO Graphs F C Focus Level Method 2 (c) 3 B 2 CDE α/2 B A A BF 3 2 D E CF F CDF 2 DF α/2 Short Focus Level C 3 3 B D 2 α A E 2 3 F CD DE CE F C D E

20 2. FWER Control within GO Graphs Table: Summary of power calculations for Simulation. Mean Node Computation n Method A B F C D E Time (sec) 5 FL SFL FL SFL FL SFL FL: Focus Level SFL: Short Focus Level

21 2. FWER Control within GO Graphs Simulation (The closure of this graph contains 574 nodes.)

22 2. FWER Control within GO Graphs Table: Results of the power analysis under Simulation 2. GO:0 GO:02 GO:03 GO:04 GO:06 GO:07 GO:0 GO: GO:3 FL SFL FL: Focus Level SFL: Short Focus Level Computation Time FL 3:42:938 SFL 0:00:05

23 2. FWER Control within GO Graphs (Computation took 3 minutes and 23 seconds. Original graph contained 5,687 nodes.) GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO: GO:00530

24 Contents Dissertation Defense Introduction 2 FWER Control within Gene Ontology Graphs 3 A Power Improving Multiplicity Correction for Large-Scale SNP Selection in LD Based QTL Mapping 4 QTL Mapping: Hypotheses and Approaches 5 Discussion

25 3. FWER Control in LD QTL Mapping Want to know if: a QTL exists, the QTL is linked to any markers.

26 3. FWER Control in LD QTL Mapping H L 0 H L 0 H L 0 H L 0 H L 0 H D 0 H D 0 H D 0 H D 0 H D 0 H0 L : No QTL exists. : QTL is unlinked with marker. H D 0

27 3. FWER Control in LD QTL Mapping H L 0 H L 0 H L 0 H L 0 H L 0 H D 0 H D 0 H D 0 H D 0 H D 0 L(p, q, D, µ,..., µ G, σ Y, M) = n G ω g Mi (p, q, D)f (Y i µ g, σ) i= g= (D is not identifiable under H L 0 )

28 3. FWER Control in LD QTL Mapping A α B H L 0 α 0 H D 0 H D 0 Figure: A) Demonstration of the GBA testing scheme for a single marker. B) The updated graph after finding H L 0 significant.

29 3. FWER Control in LD QTL Mapping α/3 α/3 α/3 H0 L H0 L2 H0 L3 /2 /2 /2 / H0 D H0 D2 H0 D3 /2 /2 Figure: Demonstration of the hierarchy of the GBA testing scheme for three markers.

30 3. FWER Control in LD QTL Mapping α/3 α/3 H D 0 H L2 0 /2 /2 0 /2 /2 H D2 0 /2 α/3 H D3 0 Figure: Demonstration of the GBA testing scheme for three markers assuming that hypotheses H0 L and H L3 0 from the initial graph in Figure 2 are rejected.

31 3. FWER Control in LD QTL Mapping A α/2 B α H L2 0 0 H D2 0 α/2 H D3 0 H L2 0 0 H D2 0 Figure: A) The updated graph from Figure 3 assuming the hypothesis H0 D of Figure 3 is rejected at the α/3-level. B) Graph resulting from the rejection of the hypothesis H D3 0 at the α/2-level.

32 3. FWER Control in LD QTL Mapping Conditions under which the GBA simplifies to an IUT (+Holm). Let H0 U denote the union hypothesis HL 0 HD 0. Let P U denote the p-value for the IUT of H0 U. Let k denote the marker with arg min P U i < α/m. Then, mp L k = P L k P D k = m max{pl k, pd k } = mpm k = P M k α where m is number of markers, p L k and pd k are raw p-values for marker k, P k are GBA adjusted p-values for marker k, and P M k denotes the raw IUT p-value for marker k.

33 3. FWER Control in LD QTL Mapping A.0 H 2 = 0. B.0 H 2 = 0.4 Power GBA Bonferroni n = 500 n = 300 n = 00 Power Number of SNPs Number of SNPs Figure: Power comparison between the graphical Bonferroni adjustment (GBA) and standard Bonferroni adjustment under different sample size, number of SNPs, and heritability (A: H 2 = 0., B: H 2 = 0.4).

34 3. FWER Control in LD QTL Mapping PC4 SNP PC4 SNP y AA Aa aa AA Aa aa Figure: The control 0.04 of leaf 0.02 shape for 0.00 different 0.02 genotypes 0.04 (AA, Aa, aa) of x the QTL identified by marker on PC 4.

35 3. FWER Control in LD QTL Mapping log p adjusted X Chromosome mb Figure: The negative log of the GBA-adjusted p-values for H0 D SNP in the mouse HDL cholesterol QTL mapping project. for each Link

36 Contents Dissertation Defense Introduction 2 FWER Control within Gene Ontology Graphs 3 A Power Improving Multiplicity Correction for Large-Scale SNP Selection in LD Based QTL Mapping 4 QTL Mapping: Hypotheses and Approaches 5 Discussion

37 4. QTL Mapping: Hypotheses and Approaches H A : a linked QTL. L(p, q, D, µ,..., µ G, σ Y, M) = H0 2 : an unlinked QTL. L(q, µ,..., µ G, σ Y) = n G ω g Mi (p, q, D)f (Y i µ g, σ). i= g= i= g= () n G ω g (q)f (Y i µ g, σ) (2) H 0 : no QTL. L(µ, σ Y) = n f (Y i µ, σ). (3) i=

38 4. QTL Mapping: Hypotheses and Approaches Test for association between QTL and phenotype Y. H L 0 : µ = µ 2 = µ 3 µ vs H L : one of the equalities above does not hold.

39 4. QTL Mapping: Hypotheses and Approaches Test for linkage between SNP and QTL. H0 D : D = 0 vs HD : D 0. (4) χ 2 D = n ˆD 2 ˆp( ˆp)ˆq( ˆq) χ2 (5)

40 4. QTL Mapping: Hypotheses and Approaches F n (x) ν = ν = 0 n=00 n=300 n= LRTS Figure: Likelihood Ratio Test of H 0 against H A for synthetic data simulated under the null hypothesis of no QTL, H 0.

41 4. QTL Mapping: Hypotheses and Approaches ν = ν = 0 no QTL known QTL unlinked QTL Figure: The empirical cumulative density functions corresponding to the test of D = 0 for three scenarios.

42 4. QTL Mapping: Hypotheses and Approaches The (Bivariate) Null Kernel Method Simulate s data sets, each of size n, based on the model assumptions of the joint hypothesis H 0. 2 Calculate T i and U i for i =,..., s. 3 Estimate the joint density ˆf of T and U using a kernel density estimation technique on the T i and U i. 4 Compute the cdf ˆF of ˆf by ˆF(c) = A(c) ˆf, where A(c) = {(t, u) ˆf (t, u) c}. 5 The joint p-value for the calculated statistics ˆt and û can then be obtained by the formula p = ˆF(ˆf (ˆt, û)).

43 4. QTL Mapping: Hypotheses and Approaches The Null Kernel Method vs. Hotelling s T 2 (bivariate test of location) T 2 = n( X µ 0 ) S ( X µ 0 ) 2(n )/(n 2)F 2,n 2 (6) U statistic T statistic Figure: Visualization of the Null Kernel method as applied to a sample of,000 T and U statistics simulated under the bivariate normal null distribution with zero mean, unit variances, and covariances of 0.3.

44 4. QTL Mapping: Hypotheses and Approaches The Null Kernel Method vs. Hotelling s T 2 (bivariate test of location) T 2 log0(p) II III I IV Null Kernel log0(p) Figure: Comparison of P-values ( log 0 (p)) obtained from either the Null Kernel method or Hotelling s T 2 test.

45 4. QTL Mapping: Hypotheses and Approaches The Null Kernel Method vs. Hotelling s T 2 (bivariate test of location) T 2 log0(p) II III I IV Null Kernel log0(p) Figure: The log 0 of the P-values from the Null Kernel and Hotelling s T 2 methods for data simulated consistent with the null hypothesis.

46 4. QTL Mapping: Hypotheses and Approaches QTL mapping Simulation Study 40 e 5 χ L χ D 2 Figure: Visualization of the Null Kernel estimated (null) density for the bivariate data corresponding to the test of H D 0, χ2 D, and HL 0, χ2 L.

47 4. QTL Mapping: Hypotheses and Approaches QTL mapping Simulation Study 0 8 Null Kernel log0(p) Chromosome Chromosome 2 Chromosome 3 Chromosome 4 Figure: The resulting adjusted P-values from each of the permutation, simulation, and theoretical approaches against the results of the Null Kernel method.

48 4. QTL Mapping: Hypotheses and Approaches Mice HDL QTL mapping study 3 log p adjusted X Chromosome mb Figure: The negative log of the Holm adjusted P-values for the Null Kernel approach.

49 4. QTL Mapping: Hypotheses and Approaches χ L χ D Figure: The joint plot of the observed test statistics for the mouse HDL QTL mapping data.

50 Contents Dissertation Defense Introduction 2 FWER Control within Gene Ontology Graphs 3 A Power Improving Multiplicity Correction for Large-Scale SNP Selection in LD Based QTL Mapping 4 QTL Mapping: Hypotheses and Approaches 5 Discussion

51 5. Discussion Dissertation Defense Professional statisticians... bear an obligation to offer alternatives (or entirely new approaches) that meet real needs and are practical as well. (J. W. Tukey, as quoted in Benjamini and Braun 200)

52 5. Discussion Dissertation Defense Introduction 2 FWER Control within Gene Ontology Graphs Extended GBA methods to Restricted Hypotheses (Theorem ). Introduced the Short Focus Level method (code in: mvgst). Quantified the computational advantage. 3 A Power Improving Multiplicity Correction for Large-Scale SNP Selection in LD Based QTL Mapping Introduced a GBA approach for LD based QTL mapping. Protects model identifiability and strong FWER control. Quantified the power increase numerically and practically. 4 QTL Mapping: Hypotheses and Approaches Detailed problems of χ 2 assumptions in LD based QTL mapping. Introduced the Null Kernel method. Showed power and computational advantages of the NK method. 5 Discussion

53 Acknowledgements Dissertation Defense This work was supported by Utah Agricultural Experiment Station (UAES) project number UTA0062, associated with the W22 multi-state project Reproductive Performance in Domestic Ruminants Utah State University VPR Research Catalyst Grant.

Family-Wise Error Rate Control in Quantitative Trait Loci (QTL) Mapping and Gene Ontology Graphs with Remarks on Family Selection

Family-Wise Error Rate Control in Quantitative Trait Loci (QTL) Mapping and Gene Ontology Graphs with Remarks on Family Selection Utah State University DigitalCommons@USU All Graduate Theses and Dissertations Graduate Studies 5-1-2014 Family-Wise Error Rate Control in Quantitative Trait Loci (QTL) Mapping and Gene Ontology Graphs

More information

Superchain Procedures in Clinical Trials. George Kordzakhia FDA, CDER, Office of Biostatistics Alex Dmitrienko Quintiles Innovation

Superchain Procedures in Clinical Trials. George Kordzakhia FDA, CDER, Office of Biostatistics Alex Dmitrienko Quintiles Innovation August 01, 2012 Disclaimer: This presentation reflects the views of the author and should not be construed to represent the views or policies of the U.S. Food and Drug Administration Introduction We describe

More information

Multiple testing: Intro & FWER 1

Multiple testing: Intro & FWER 1 Multiple testing: Intro & FWER 1 Mark van de Wiel mark.vdwiel@vumc.nl Dep of Epidemiology & Biostatistics,VUmc, Amsterdam Dep of Mathematics, VU 1 Some slides courtesy of Jelle Goeman 1 Practical notes

More information

High-Throughput Sequencing Course. Introduction. Introduction. Multiple Testing. Biostatistics and Bioinformatics. Summer 2018

High-Throughput Sequencing Course. Introduction. Introduction. Multiple Testing. Biostatistics and Bioinformatics. Summer 2018 High-Throughput Sequencing Course Multiple Testing Biostatistics and Bioinformatics Summer 2018 Introduction You have previously considered the significance of a single gene Introduction You have previously

More information

Mixtures of multiple testing procedures for gatekeeping applications in clinical trials

Mixtures of multiple testing procedures for gatekeeping applications in clinical trials Research Article Received 29 January 2010, Accepted 26 May 2010 Published online 18 April 2011 in Wiley Online Library (wileyonlinelibrary.com) DOI: 10.1002/sim.4008 Mixtures of multiple testing procedures

More information

A NEW APPROACH FOR LARGE SCALE MULTIPLE TESTING WITH APPLICATION TO FDR CONTROL FOR GRAPHICALLY STRUCTURED HYPOTHESES

A NEW APPROACH FOR LARGE SCALE MULTIPLE TESTING WITH APPLICATION TO FDR CONTROL FOR GRAPHICALLY STRUCTURED HYPOTHESES A NEW APPROACH FOR LARGE SCALE MULTIPLE TESTING WITH APPLICATION TO FDR CONTROL FOR GRAPHICALLY STRUCTURED HYPOTHESES By Wenge Guo Gavin Lynch Joseph P. Romano Technical Report No. 2018-06 September 2018

More information

Step-down FDR Procedures for Large Numbers of Hypotheses

Step-down FDR Procedures for Large Numbers of Hypotheses Step-down FDR Procedures for Large Numbers of Hypotheses Paul N. Somerville University of Central Florida Abstract. Somerville (2004b) developed FDR step-down procedures which were particularly appropriate

More information

Advanced Statistical Methods: Beyond Linear Regression

Advanced Statistical Methods: Beyond Linear Regression Advanced Statistical Methods: Beyond Linear Regression John R. Stevens Utah State University Notes 3. Statistical Methods II Mathematics Educators Worshop 28 March 2009 1 http://www.stat.usu.edu/~jrstevens/pcmi

More information

Familywise Error Rate Controlling Procedures for Discrete Data

Familywise Error Rate Controlling Procedures for Discrete Data Familywise Error Rate Controlling Procedures for Discrete Data arxiv:1711.08147v1 [stat.me] 22 Nov 2017 Yalin Zhu Center for Mathematical Sciences, Merck & Co., Inc., West Point, PA, U.S.A. Wenge Guo Department

More information

Testing a secondary endpoint after a group sequential test. Chris Jennison. 9th Annual Adaptive Designs in Clinical Trials

Testing a secondary endpoint after a group sequential test. Chris Jennison. 9th Annual Adaptive Designs in Clinical Trials Testing a secondary endpoint after a group sequential test Christopher Jennison Department of Mathematical Sciences, University of Bath, UK http://people.bath.ac.uk/mascj 9th Annual Adaptive Designs in

More information

High-throughput Testing

High-throughput Testing High-throughput Testing Noah Simon and Richard Simon July 2016 1 / 29 Testing vs Prediction On each of n patients measure y i - single binary outcome (eg. progression after a year, PCR) x i - p-vector

More information

On Generalized Fixed Sequence Procedures for Controlling the FWER

On Generalized Fixed Sequence Procedures for Controlling the FWER Research Article Received XXXX (www.interscience.wiley.com) DOI: 10.1002/sim.0000 On Generalized Fixed Sequence Procedures for Controlling the FWER Zhiying Qiu, a Wenge Guo b and Gavin Lynch c Testing

More information

False discovery rate control for non-positively regression dependent test statistics

False discovery rate control for non-positively regression dependent test statistics Journal of Statistical Planning and Inference ( ) www.elsevier.com/locate/jspi False discovery rate control for non-positively regression dependent test statistics Daniel Yekutieli Department of Statistics

More information

Lecture 6 April

Lecture 6 April Stats 300C: Theory of Statistics Spring 2017 Lecture 6 April 14 2017 Prof. Emmanuel Candes Scribe: S. Wager, E. Candes 1 Outline Agenda: From global testing to multiple testing 1. Testing the global null

More information

Summary and discussion of: Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

Summary and discussion of: Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing Summary and discussion of: Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing Statistics Journal Club, 36-825 Beau Dabbs and Philipp Burckhardt 9-19-2014 1 Paper

More information

Multiple Testing. Hoang Tran. Department of Statistics, Florida State University

Multiple Testing. Hoang Tran. Department of Statistics, Florida State University Multiple Testing Hoang Tran Department of Statistics, Florida State University Large-Scale Testing Examples: Microarray data: testing differences in gene expression between two traits/conditions Microbiome

More information

Looking at the Other Side of Bonferroni

Looking at the Other Side of Bonferroni Department of Biostatistics University of Washington 24 May 2012 Multiple Testing: Control the Type I Error Rate When analyzing genetic data, one will commonly perform over 1 million (and growing) hypothesis

More information

Stat 206: Estimation and testing for a mean vector,

Stat 206: Estimation and testing for a mean vector, Stat 206: Estimation and testing for a mean vector, Part II James Johndrow 2016-12-03 Comparing components of the mean vector In the last part, we talked about testing the hypothesis H 0 : µ 1 = µ 2 where

More information

Statistical Applications in Genetics and Molecular Biology

Statistical Applications in Genetics and Molecular Biology Statistical Applications in Genetics and Molecular Biology Volume 5, Issue 1 2006 Article 28 A Two-Step Multiple Comparison Procedure for a Large Number of Tests and Multiple Treatments Hongmei Jiang Rebecca

More information

Lecture 28. Ingo Ruczinski. December 3, Department of Biostatistics Johns Hopkins Bloomberg School of Public Health Johns Hopkins University

Lecture 28. Ingo Ruczinski. December 3, Department of Biostatistics Johns Hopkins Bloomberg School of Public Health Johns Hopkins University Lecture 28 Department of Biostatistics Johns Hopkins Bloomberg School of Public Health Johns Hopkins University December 3, 2015 1 2 3 4 5 1 Familywise error rates 2 procedure 3 Performance of with multiple

More information

STAT 5200 Handout #7a Contrasts & Post hoc Means Comparisons (Ch. 4-5)

STAT 5200 Handout #7a Contrasts & Post hoc Means Comparisons (Ch. 4-5) STAT 5200 Handout #7a Contrasts & Post hoc Means Comparisons Ch. 4-5) Recall CRD means and effects models: Y ij = µ i + ϵ ij = µ + α i + ϵ ij i = 1,..., g ; j = 1,..., n ; ϵ ij s iid N0, σ 2 ) If we reject

More information

Multiple Endpoints: A Review and New. Developments. Ajit C. Tamhane. (Joint work with Brent R. Logan) Department of IE/MS and Statistics

Multiple Endpoints: A Review and New. Developments. Ajit C. Tamhane. (Joint work with Brent R. Logan) Department of IE/MS and Statistics 1 Multiple Endpoints: A Review and New Developments Ajit C. Tamhane (Joint work with Brent R. Logan) Department of IE/MS and Statistics Northwestern University Evanston, IL 60208 ajit@iems.northwestern.edu

More information

Control of Directional Errors in Fixed Sequence Multiple Testing

Control of Directional Errors in Fixed Sequence Multiple Testing Control of Directional Errors in Fixed Sequence Multiple Testing Anjana Grandhi Department of Mathematical Sciences New Jersey Institute of Technology Newark, NJ 07102-1982 Wenge Guo Department of Mathematical

More information

Statistical testing. Samantha Kleinberg. October 20, 2009

Statistical testing. Samantha Kleinberg. October 20, 2009 October 20, 2009 Intro to significance testing Significance testing and bioinformatics Gene expression: Frequently have microarray data for some group of subjects with/without the disease. Want to find

More information

Control of Generalized Error Rates in Multiple Testing

Control of Generalized Error Rates in Multiple Testing Institute for Empirical Research in Economics University of Zurich Working Paper Series ISSN 1424-0459 Working Paper No. 245 Control of Generalized Error Rates in Multiple Testing Joseph P. Romano and

More information

MULTISTAGE AND MIXTURE PARALLEL GATEKEEPING PROCEDURES IN CLINICAL TRIALS

MULTISTAGE AND MIXTURE PARALLEL GATEKEEPING PROCEDURES IN CLINICAL TRIALS Journal of Biopharmaceutical Statistics, 21: 726 747, 2011 Copyright Taylor & Francis Group, LLC ISSN: 1054-3406 print/1520-5711 online DOI: 10.1080/10543406.2011.551333 MULTISTAGE AND MIXTURE PARALLEL

More information

Non-specific filtering and control of false positives

Non-specific filtering and control of false positives Non-specific filtering and control of false positives Richard Bourgon 16 June 2009 bourgon@ebi.ac.uk EBI is an outstation of the European Molecular Biology Laboratory Outline Multiple testing I: overview

More information

Applying the Benjamini Hochberg procedure to a set of generalized p-values

Applying the Benjamini Hochberg procedure to a set of generalized p-values U.U.D.M. Report 20:22 Applying the Benjamini Hochberg procedure to a set of generalized p-values Fredrik Jonsson Department of Mathematics Uppsala University Applying the Benjamini Hochberg procedure

More information

False discovery rate and related concepts in multiple comparisons problems, with applications to microarray data

False discovery rate and related concepts in multiple comparisons problems, with applications to microarray data False discovery rate and related concepts in multiple comparisons problems, with applications to microarray data Ståle Nygård Trial Lecture Dec 19, 2008 1 / 35 Lecture outline Motivation for not using

More information

Adaptive, graph based multiple testing procedures and a uniform improvement of Bonferroni type tests.

Adaptive, graph based multiple testing procedures and a uniform improvement of Bonferroni type tests. 1/35 Adaptive, graph based multiple testing procedures and a uniform improvement of Bonferroni type tests. Martin Posch Center for Medical Statistics, Informatics and Intelligent Systems Medical University

More information

Sample Size Estimation for Studies of High-Dimensional Data

Sample Size Estimation for Studies of High-Dimensional Data Sample Size Estimation for Studies of High-Dimensional Data James J. Chen, Ph.D. National Center for Toxicological Research Food and Drug Administration June 3, 2009 China Medical University Taichung,

More information

Compatible simultaneous lower confidence bounds for the Holm procedure and other Bonferroni based closed tests

Compatible simultaneous lower confidence bounds for the Holm procedure and other Bonferroni based closed tests Compatible simultaneous lower confidence bounds for the Holm procedure and other Bonferroni based closed tests K. Strassburger 1, F. Bretz 2 1 Institute of Biometrics & Epidemiology German Diabetes Center,

More information

Fall 2017 STAT 532 Homework Peter Hoff. 1. Let P be a probability measure on a collection of sets A.

Fall 2017 STAT 532 Homework Peter Hoff. 1. Let P be a probability measure on a collection of sets A. 1. Let P be a probability measure on a collection of sets A. (a) For each n N, let H n be a set in A such that H n H n+1. Show that P (H n ) monotonically converges to P ( k=1 H k) as n. (b) For each n

More information

Chapter Seven: Multi-Sample Methods 1/52

Chapter Seven: Multi-Sample Methods 1/52 Chapter Seven: Multi-Sample Methods 1/52 7.1 Introduction 2/52 Introduction The independent samples t test and the independent samples Z test for a difference between proportions are designed to analyze

More information

On Procedures Controlling the FDR for Testing Hierarchically Ordered Hypotheses

On Procedures Controlling the FDR for Testing Hierarchically Ordered Hypotheses On Procedures Controlling the FDR for Testing Hierarchically Ordered Hypotheses Gavin Lynch Catchpoint Systems, Inc., 228 Park Ave S 28080 New York, NY 10003, U.S.A. Wenge Guo Department of Mathematical

More information

A TUTORIAL ON THE INHERITANCE PROCEDURE FOR MULTIPLE TESTING OF TREE-STRUCTURED HYPOTHESES

A TUTORIAL ON THE INHERITANCE PROCEDURE FOR MULTIPLE TESTING OF TREE-STRUCTURED HYPOTHESES A TUTORIAL ON THE INHERITANCE PROCEDURE FOR MULTIPLE TESTING OF TREE-STRUCTURED HYPOTHESES by Dilinuer Kuerban B.Sc. (Statistics), Southwestern University of Finance & Economics, 2011 a Project submitted

More information

Modified Simes Critical Values Under Positive Dependence

Modified Simes Critical Values Under Positive Dependence Modified Simes Critical Values Under Positive Dependence Gengqian Cai, Sanat K. Sarkar Clinical Pharmacology Statistics & Programming, BDS, GlaxoSmithKline Statistics Department, Temple University, Philadelphia

More information

Table of Outcomes. Table of Outcomes. Table of Outcomes. Table of Outcomes. Table of Outcomes. Table of Outcomes. T=number of type 2 errors

Table of Outcomes. Table of Outcomes. Table of Outcomes. Table of Outcomes. Table of Outcomes. Table of Outcomes. T=number of type 2 errors The Multiple Testing Problem Multiple Testing Methods for the Analysis of Microarray Data 3/9/2009 Copyright 2009 Dan Nettleton Suppose one test of interest has been conducted for each of m genes in a

More information

ON STEPWISE CONTROL OF THE GENERALIZED FAMILYWISE ERROR RATE. By Wenge Guo and M. Bhaskara Rao

ON STEPWISE CONTROL OF THE GENERALIZED FAMILYWISE ERROR RATE. By Wenge Guo and M. Bhaskara Rao ON STEPWISE CONTROL OF THE GENERALIZED FAMILYWISE ERROR RATE By Wenge Guo and M. Bhaskara Rao National Institute of Environmental Health Sciences and University of Cincinnati A classical approach for dealing

More information

Lecture 27. December 13, Department of Biostatistics Johns Hopkins Bloomberg School of Public Health Johns Hopkins University.

Lecture 27. December 13, Department of Biostatistics Johns Hopkins Bloomberg School of Public Health Johns Hopkins University. This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike License. Your use of this material constitutes acceptance of that license and the conditions of use of materials on this

More information

Lecture 21: October 19

Lecture 21: October 19 36-705: Intermediate Statistics Fall 2017 Lecturer: Siva Balakrishnan Lecture 21: October 19 21.1 Likelihood Ratio Test (LRT) To test composite versus composite hypotheses the general method is to use

More information

On adaptive procedures controlling the familywise error rate

On adaptive procedures controlling the familywise error rate , pp. 3 On adaptive procedures controlling the familywise error rate By SANAT K. SARKAR Temple University, Philadelphia, PA 922, USA sanat@temple.edu Summary This paper considers the problem of developing

More information

The Design of Group Sequential Clinical Trials that Test Multiple Endpoints

The Design of Group Sequential Clinical Trials that Test Multiple Endpoints The Design of Group Sequential Clinical Trials that Test Multiple Endpoints Christopher Jennison Department of Mathematical Sciences, University of Bath, UK http://people.bath.ac.uk/mascj Bruce Turnbull

More information

Hochberg Multiple Test Procedure Under Negative Dependence

Hochberg Multiple Test Procedure Under Negative Dependence Hochberg Multiple Test Procedure Under Negative Dependence Ajit C. Tamhane Northwestern University Joint work with Jiangtao Gou (Northwestern University) IMPACT Symposium, Cary (NC), November 20, 2014

More information

One-week Course on Genetic Analysis and Plant Breeding January 2013, CIMMYT, Mexico LOD Threshold and QTL Detection Power Simulation

One-week Course on Genetic Analysis and Plant Breeding January 2013, CIMMYT, Mexico LOD Threshold and QTL Detection Power Simulation One-week Course on Genetic Analysis and Plant Breeding 21-2 January 213, CIMMYT, Mexico LOD Threshold and QTL Detection Power Simulation Jiankang Wang, CIMMYT China and CAAS E-mail: jkwang@cgiar.org; wangjiankang@caas.cn

More information

Multiple Testing of General Contrasts: Truncated Closure and the Extended Shaffer-Royen Method

Multiple Testing of General Contrasts: Truncated Closure and the Extended Shaffer-Royen Method Multiple Testing of General Contrasts: Truncated Closure and the Extended Shaffer-Royen Method Peter H. Westfall, Texas Tech University Randall D. Tobias, SAS Institute Pairwise Comparisons ANOVA, g =10groups,

More information

FDR-CONTROLLING STEPWISE PROCEDURES AND THEIR FALSE NEGATIVES RATES

FDR-CONTROLLING STEPWISE PROCEDURES AND THEIR FALSE NEGATIVES RATES FDR-CONTROLLING STEPWISE PROCEDURES AND THEIR FALSE NEGATIVES RATES Sanat K. Sarkar a a Department of Statistics, Temple University, Speakman Hall (006-00), Philadelphia, PA 19122, USA Abstract The concept

More information

Statistica Sinica Preprint No: SS R1

Statistica Sinica Preprint No: SS R1 Statistica Sinica Preprint No: SS-2017-0072.R1 Title Control of Directional Errors in Fixed Sequence Multiple Testing Manuscript ID SS-2017-0072.R1 URL http://www.stat.sinica.edu.tw/statistica/ DOI 10.5705/ss.202017.0072

More information

A note on tree gatekeeping procedures in clinical trials

A note on tree gatekeeping procedures in clinical trials STATISTICS IN MEDICINE Statist. Med. 2008; 06:1 6 [Version: 2002/09/18 v1.11] A note on tree gatekeeping procedures in clinical trials Alex Dmitrienko 1, Ajit C. Tamhane 2, Lingyun Liu 2, Brian L. Wiens

More information

Controlling the False Discovery Rate: Understanding and Extending the Benjamini-Hochberg Method

Controlling the False Discovery Rate: Understanding and Extending the Benjamini-Hochberg Method Controlling the False Discovery Rate: Understanding and Extending the Benjamini-Hochberg Method Christopher R. Genovese Department of Statistics Carnegie Mellon University joint work with Larry Wasserman

More information

Journal Club: Higher Criticism

Journal Club: Higher Criticism Journal Club: Higher Criticism David Donoho (2002): Higher Criticism for Heterogeneous Mixtures, Technical Report No. 2002-12, Dept. of Statistics, Stanford University. Introduction John Tukey (1976):

More information

Resampling-based Multiple Testing with Applications to Microarray Data Analysis

Resampling-based Multiple Testing with Applications to Microarray Data Analysis Resampling-based Multiple Testing with Applications to Microarray Data Analysis DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School

More information

Closure properties of classes of multiple testing procedures

Closure properties of classes of multiple testing procedures AStA Adv Stat Anal (2018) 102:167 178 https://doi.org/10.1007/s10182-017-0297-0 ORIGINAL PAPER Closure properties of classes of multiple testing procedures Georg Hahn 1 Received: 28 June 2016 / Accepted:

More information

A Mixture Gatekeeping Procedure Based on the Hommel Test for Clinical Trial Applications

A Mixture Gatekeeping Procedure Based on the Hommel Test for Clinical Trial Applications A Mixture Gatekeeping Procedure Based on the Hommel Test for Clinical Trial Applications Thomas Brechenmacher (Dainippon Sumitomo Pharma Co., Ltd.) Jane Xu (Sunovion Pharmaceuticals Inc.) Alex Dmitrienko

More information

PB HLTH 240A: Advanced Categorical Data Analysis Fall 2007

PB HLTH 240A: Advanced Categorical Data Analysis Fall 2007 Cohort study s formulations PB HLTH 240A: Advanced Categorical Data Analysis Fall 2007 Srine Dudoit Division of Biostatistics Department of Statistics University of California, Berkeley www.stat.berkeley.edu/~srine

More information

STAT 263/363: Experimental Design Winter 2016/17. Lecture 1 January 9. Why perform Design of Experiments (DOE)? There are at least two reasons:

STAT 263/363: Experimental Design Winter 2016/17. Lecture 1 January 9. Why perform Design of Experiments (DOE)? There are at least two reasons: STAT 263/363: Experimental Design Winter 206/7 Lecture January 9 Lecturer: Minyong Lee Scribe: Zachary del Rosario. Design of Experiments Why perform Design of Experiments (DOE)? There are at least two

More information

Bonferroni - based gatekeeping procedure with retesting option

Bonferroni - based gatekeeping procedure with retesting option Bonferroni - based gatekeeping procedure with retesting option Zhiying Qiu Biostatistics and Programming, Sanofi Bridgewater, NJ 08807, U.S.A. Wenge Guo Department of Mathematical Sciences New Jersey Institute

More information

Statistical Applications in Genetics and Molecular Biology

Statistical Applications in Genetics and Molecular Biology Statistical Applications in Genetics and Molecular Biology Volume 3, Issue 1 2004 Article 13 Multiple Testing. Part I. Single-Step Procedures for Control of General Type I Error Rates Sandrine Dudoit Mark

More information

PROCEDURES CONTROLLING THE k-fdr USING. BIVARIATE DISTRIBUTIONS OF THE NULL p-values. Sanat K. Sarkar and Wenge Guo

PROCEDURES CONTROLLING THE k-fdr USING. BIVARIATE DISTRIBUTIONS OF THE NULL p-values. Sanat K. Sarkar and Wenge Guo PROCEDURES CONTROLLING THE k-fdr USING BIVARIATE DISTRIBUTIONS OF THE NULL p-values Sanat K. Sarkar and Wenge Guo Temple University and National Institute of Environmental Health Sciences Abstract: Procedures

More information

Exact and Approximate Stepdown Methods For Multiple Hypothesis Testing

Exact and Approximate Stepdown Methods For Multiple Hypothesis Testing Exact and Approximate Stepdown Methods For Multiple Hypothesis Testing Joseph P. Romano Department of Statistics Stanford University Michael Wolf Department of Economics and Business Universitat Pompeu

More information

Zhiguang Huo 1, Chi Song 2, George Tseng 3. July 30, 2018

Zhiguang Huo 1, Chi Song 2, George Tseng 3. July 30, 2018 Bayesian latent hierarchical model for transcriptomic meta-analysis to detect biomarkers with clustered meta-patterns of differential expression signals BayesMP Zhiguang Huo 1, Chi Song 2, George Tseng

More information

MODEL-FREE LINKAGE AND ASSOCIATION MAPPING OF COMPLEX TRAITS USING QUANTITATIVE ENDOPHENOTYPES

MODEL-FREE LINKAGE AND ASSOCIATION MAPPING OF COMPLEX TRAITS USING QUANTITATIVE ENDOPHENOTYPES MODEL-FREE LINKAGE AND ASSOCIATION MAPPING OF COMPLEX TRAITS USING QUANTITATIVE ENDOPHENOTYPES Saurabh Ghosh Human Genetics Unit Indian Statistical Institute, Kolkata Most common diseases are caused by

More information

Group sequential designs for Clinical Trials with multiple treatment arms

Group sequential designs for Clinical Trials with multiple treatment arms Group sequential designs for Clinical Trials with multiple treatment arms Susanne Urach, Martin Posch Cologne, June 26, 2015 This project has received funding from the European Union s Seventh Framework

More information

arxiv: v1 [math.st] 14 Nov 2012

arxiv: v1 [math.st] 14 Nov 2012 The Annals of Statistics 2010, Vol. 38, No. 6, 3782 3810 DOI: 10.1214/10-AOS829 c Institute of Mathematical Statistics, 2010 arxiv:1211.3313v1 [math.st] 14 Nov 2012 THE SEQUENTIAL REJECTION PRINCIPLE OF

More information

Association studies and regression

Association studies and regression Association studies and regression CM226: Machine Learning for Bioinformatics. Fall 2016 Sriram Sankararaman Acknowledgments: Fei Sha, Ameet Talwalkar Association studies and regression 1 / 104 Administration

More information

Some General Types of Tests

Some General Types of Tests Some General Types of Tests We may not be able to find a UMP or UMPU test in a given situation. In that case, we may use test of some general class of tests that often have good asymptotic properties.

More information

Week 5 Video 1 Relationship Mining Correlation Mining

Week 5 Video 1 Relationship Mining Correlation Mining Week 5 Video 1 Relationship Mining Correlation Mining Relationship Mining Discover relationships between variables in a data set with many variables Many types of relationship mining Correlation Mining

More information

Model Identification for Wireless Propagation with Control of the False Discovery Rate

Model Identification for Wireless Propagation with Control of the False Discovery Rate Model Identification for Wireless Propagation with Control of the False Discovery Rate Christoph F. Mecklenbräuker (TU Wien) Joint work with Pei-Jung Chung (Univ. Edinburgh) Dirk Maiwald (Atlas Elektronik)

More information

Linear Combinations. Comparison of treatment means. Bruce A Craig. Department of Statistics Purdue University. STAT 514 Topic 6 1

Linear Combinations. Comparison of treatment means. Bruce A Craig. Department of Statistics Purdue University. STAT 514 Topic 6 1 Linear Combinations Comparison of treatment means Bruce A Craig Department of Statistics Purdue University STAT 514 Topic 6 1 Linear Combinations of Means y ij = µ + τ i + ǫ ij = µ i + ǫ ij Often study

More information

Estimation of a Two-component Mixture Model

Estimation of a Two-component Mixture Model Estimation of a Two-component Mixture Model Bodhisattva Sen 1,2 University of Cambridge, Cambridge, UK Columbia University, New York, USA Indian Statistical Institute, Kolkata, India 6 August, 2012 1 Joint

More information

False Discovery Rate

False Discovery Rate False Discovery Rate Peng Zhao Department of Statistics Florida State University December 3, 2018 Peng Zhao False Discovery Rate 1/30 Outline 1 Multiple Comparison and FWER 2 False Discovery Rate 3 FDR

More information

Biostatistics Advanced Methods in Biostatistics IV

Biostatistics Advanced Methods in Biostatistics IV Biostatistics 140.754 Advanced Methods in Biostatistics IV Jeffrey Leek Assistant Professor Department of Biostatistics jleek@jhsph.edu Lecture 11 1 / 44 Tip + Paper Tip: Two today: (1) Graduate school

More information

Lecture 13: p-values and union intersection tests

Lecture 13: p-values and union intersection tests Lecture 13: p-values and union intersection tests p-values After a hypothesis test is done, one method of reporting the result is to report the size α of the test used to reject H 0 or accept H 0. If α

More information

Multiple Testing of One-Sided Hypotheses: Combining Bonferroni and the Bootstrap

Multiple Testing of One-Sided Hypotheses: Combining Bonferroni and the Bootstrap University of Zurich Department of Economics Working Paper Series ISSN 1664-7041 (print) ISSN 1664-705X (online) Working Paper No. 254 Multiple Testing of One-Sided Hypotheses: Combining Bonferroni and

More information

Peak Detection for Images

Peak Detection for Images Peak Detection for Images Armin Schwartzman Division of Biostatistics, UC San Diego June 016 Overview How can we improve detection power? Use a less conservative error criterion Take advantage of prior

More information

Multiple Testing. Gary W. Oehlert. January 28, School of Statistics University of Minnesota

Multiple Testing. Gary W. Oehlert. January 28, School of Statistics University of Minnesota Multiple Testing Gary W. Oehlert School of Statistics University of Minnesota January 28, 2016 Background Suppose that you had a 20-sided die. Nineteen of the sides are labeled 0 and one of the sides is

More information

STAT 461/561- Assignments, Year 2015

STAT 461/561- Assignments, Year 2015 STAT 461/561- Assignments, Year 2015 This is the second set of assignment problems. When you hand in any problem, include the problem itself and its number. pdf are welcome. If so, use large fonts and

More information

Multiple comparisons of slopes of regression lines. Jolanta Wojnar, Wojciech Zieliński

Multiple comparisons of slopes of regression lines. Jolanta Wojnar, Wojciech Zieliński Multiple comparisons of slopes of regression lines Jolanta Wojnar, Wojciech Zieliński Institute of Statistics and Econometrics University of Rzeszów ul Ćwiklińskiej 2, 35-61 Rzeszów e-mail: jwojnar@univrzeszowpl

More information

INTRODUCTION TO INTERSECTION-UNION TESTS

INTRODUCTION TO INTERSECTION-UNION TESTS INTRODUCTION TO INTERSECTION-UNION TESTS Jimmy A. Doi, Cal Poly State University San Luis Obispo Department of Statistics (jdoi@calpoly.edu Key Words: Intersection-Union Tests; Multiple Comparisons; Acceptance

More information

STAT22200 Spring 2014 Chapter 5

STAT22200 Spring 2014 Chapter 5 STAT22200 Spring 2014 Chapter 5 Yibi Huang April 29, 2014 Chapter 5 Multiple Comparisons Chapter 5-1 Chapter 5 Multiple Comparisons Note the t-tests and C.I. s are constructed assuming we only do one test,

More information

University of California, Berkeley

University of California, Berkeley University of California, Berkeley U.C. Berkeley Division of Biostatistics Working Paper Series Year 2004 Paper 164 Multiple Testing Procedures: R multtest Package and Applications to Genomics Katherine

More information

A class of improved hybrid Hochberg Hommel type step-up multiple test procedures

A class of improved hybrid Hochberg Hommel type step-up multiple test procedures Biometrika (2014), 101,4,pp. 899 911 doi: 10.1093/biomet/asu032 Printed in Great Britain Advance Access publication 24 October 2014 A class of improved hybrid Hochberg Hommel type step-up multiple test

More information

Statistical Inference

Statistical Inference Statistical Inference Classical and Bayesian Methods Class 6 AMS-UCSC Thu 26, 2012 Winter 2012. Session 1 (Class 6) AMS-132/206 Thu 26, 2012 1 / 15 Topics Topics We will talk about... 1 Hypothesis testing

More information

are equal to zero, where, q = p 1. For each gene j, the pairwise null and alternative hypotheses are,

are equal to zero, where, q = p 1. For each gene j, the pairwise null and alternative hypotheses are, Page of 8 Suppleentary Materials: A ultiple testing procedure for ulti-diensional pairwise coparisons with application to gene expression studies Anjana Grandhi, Wenge Guo, Shyaal D. Peddada S Notations

More information

Sta$s$cs for Genomics ( )

Sta$s$cs for Genomics ( ) Sta$s$cs for Genomics (140.688) Instructor: Jeff Leek Slide Credits: Rafael Irizarry, John Storey No announcements today. Hypothesis testing Once you have a given score for each gene, how do you decide

More information

The International Journal of Biostatistics

The International Journal of Biostatistics The International Journal of Biostatistics Volume 7, Issue 1 2011 Article 12 Consonance and the Closure Method in Multiple Testing Joseph P. Romano, Stanford University Azeem Shaikh, University of Chicago

More information

Multiple QTL mapping

Multiple QTL mapping Multiple QTL mapping Karl W Broman Department of Biostatistics Johns Hopkins University www.biostat.jhsph.edu/~kbroman [ Teaching Miscellaneous lectures] 1 Why? Reduce residual variation = increased power

More information

Type I error rate control in adaptive designs for confirmatory clinical trials with treatment selection at interim

Type I error rate control in adaptive designs for confirmatory clinical trials with treatment selection at interim Type I error rate control in adaptive designs for confirmatory clinical trials with treatment selection at interim Frank Bretz Statistical Methodology, Novartis Joint work with Martin Posch (Medical University

More information

Alpha-Investing. Sequential Control of Expected False Discoveries

Alpha-Investing. Sequential Control of Expected False Discoveries Alpha-Investing Sequential Control of Expected False Discoveries Dean Foster Bob Stine Department of Statistics Wharton School of the University of Pennsylvania www-stat.wharton.upenn.edu/ stine Joint

More information

Exam: high-dimensional data analysis January 20, 2014

Exam: high-dimensional data analysis January 20, 2014 Exam: high-dimensional data analysis January 20, 204 Instructions: - Write clearly. Scribbles will not be deciphered. - Answer each main question not the subquestions on a separate piece of paper. - Finish

More information

A Sequential Bayesian Approach with Applications to Circadian Rhythm Microarray Gene Expression Data

A Sequential Bayesian Approach with Applications to Circadian Rhythm Microarray Gene Expression Data A Sequential Bayesian Approach with Applications to Circadian Rhythm Microarray Gene Expression Data Faming Liang, Chuanhai Liu, and Naisyin Wang Texas A&M University Multiple Hypothesis Testing Introduction

More information

Multiple Testing. Tim Hanson. January, Modified from originals by Gary W. Oehlert. Department of Statistics University of South Carolina

Multiple Testing. Tim Hanson. January, Modified from originals by Gary W. Oehlert. Department of Statistics University of South Carolina Multiple Testing Tim Hanson Department of Statistics University of South Carolina January, 2017 Modified from originals by Gary W. Oehlert Type I error A Type I error is to wrongly reject the null hypothesis

More information

STAT 135 Lab 9 Multiple Testing, One-Way ANOVA and Kruskal-Wallis

STAT 135 Lab 9 Multiple Testing, One-Way ANOVA and Kruskal-Wallis STAT 135 Lab 9 Multiple Testing, One-Way ANOVA and Kruskal-Wallis Rebecca Barter April 6, 2015 Multiple Testing Multiple Testing Recall that when we were doing two sample t-tests, we were testing the equality

More information

Causal Model Selection Hypothesis Tests in Systems Genetics

Causal Model Selection Hypothesis Tests in Systems Genetics 1 Causal Model Selection Hypothesis Tests in Systems Genetics Elias Chaibub Neto and Brian S Yandell SISG 2012 July 13, 2012 2 Correlation and Causation The old view of cause and effect... could only fail;

More information

How to analyze many contingency tables simultaneously?

How to analyze many contingency tables simultaneously? How to analyze many contingency tables simultaneously? Thorsten Dickhaus Humboldt-Universität zu Berlin Beuth Hochschule für Technik Berlin, 31.10.2012 Outline Motivation: Genetic association studies Statistical

More information

Statistical Applications in Genetics and Molecular Biology

Statistical Applications in Genetics and Molecular Biology Statistical Applications in Genetics and Molecular Biology Volume 6, Issue 1 2007 Article 28 A Comparison of Methods to Control Type I Errors in Microarray Studies Jinsong Chen Mark J. van der Laan Martyn

More information

MULTIPLE TESTING PROCEDURES AND SIMULTANEOUS INTERVAL ESTIMATES WITH THE INTERVAL PROPERTY

MULTIPLE TESTING PROCEDURES AND SIMULTANEOUS INTERVAL ESTIMATES WITH THE INTERVAL PROPERTY MULTIPLE TESTING PROCEDURES AND SIMULTANEOUS INTERVAL ESTIMATES WITH THE INTERVAL PROPERTY BY YINGQIU MA A dissertation submitted to the Graduate School New Brunswick Rutgers, The State University of New

More information

Controlling Bayes Directional False Discovery Rate in Random Effects Model 1

Controlling Bayes Directional False Discovery Rate in Random Effects Model 1 Controlling Bayes Directional False Discovery Rate in Random Effects Model 1 Sanat K. Sarkar a, Tianhui Zhou b a Temple University, Philadelphia, PA 19122, USA b Wyeth Pharmaceuticals, Collegeville, PA

More information

Let us first identify some classes of hypotheses. simple versus simple. H 0 : θ = θ 0 versus H 1 : θ = θ 1. (1) one-sided

Let us first identify some classes of hypotheses. simple versus simple. H 0 : θ = θ 0 versus H 1 : θ = θ 1. (1) one-sided Let us first identify some classes of hypotheses. simple versus simple H 0 : θ = θ 0 versus H 1 : θ = θ 1. (1) one-sided H 0 : θ θ 0 versus H 1 : θ > θ 0. (2) two-sided; null on extremes H 0 : θ θ 1 or

More information

Adaptive Extensions of a Two-Stage Group Sequential Procedure for Testing a Primary and a Secondary Endpoint (II): Sample Size Re-estimation

Adaptive Extensions of a Two-Stage Group Sequential Procedure for Testing a Primary and a Secondary Endpoint (II): Sample Size Re-estimation Research Article Received XXXX (www.interscience.wiley.com) DOI: 10.100/sim.0000 Adaptive Extensions of a Two-Stage Group Sequential Procedure for Testing a Primary and a Secondary Endpoint (II): Sample

More information