Type I and Type II error rates for quantitative trait loci (QTL) mapping studies using recombinant inbred mouse strains

被引:143
作者
Belknap, JK [1 ]
Mitchell, SR [1 ]
OToole, LA [1 ]
Helms, ML [1 ]
Crabbe, JC [1 ]
机构
[1] OREGON HLTH SCI UNIV,DEPT MED PSYCHOL,PORTLAND,OR 97201
关键词
QTL mapping; recombinant inbred strains; C57BL/6; DBA/2; BXD;
D O I
10.1007/BF02359892
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 [法学]; 0303 [社会学]; 030303 [人类学]; 04 [教育学]; 0402 [心理学];
摘要
Effective mapping strategies for quantitative traits must allow for the detection of the more important quantitative trait loci (QTLs) while minimizing false positives. Type I (false-positive) and Type II (false-negative) error rates were estimated from a computer simulation of QTL mapping in the BXD recombinant inbred (RI) set comprising 26 strains of mice, and comparisons made with theoretical predictions. The results are generally applicable to other RI sets when corrections are made for differing strain numbers and marker densities. Regardless of the number or magnitude of simulated QTLs contributing to the trait variance, the p value necessary to provide genome-wide .05 Type I error protection was found to be about p = .0001. To provide adequate protection against both Type I (alpha = .0001) and Type II (beta = .2) errors, a QTL would have to account for more than half of the between-strain (genetic) variance if the BXD or similar set was used alone. In contrast, a two-step mapping strategy was also considered, where RI strains are used as a preliminary screen for QTLs to be specifically tested (confirmed) in an F-2 (or other) population. In this case, QTLs accounting for similar to 16% of the between-strain variance could be detected with an 80% probability in the BXD set when alpha = 0.2. To balance the competing goals of minimizing Type I and II errors, an economical strategy is to adopt a more stringent alpha initially for the RI screen, since this requires only a limited genome search in the F-2 of the RI-implicated regions (similar to 10% of the F-2 genome when p < .01 in the RIs). If confirmed QTLs do not account in the aggregate for a sufficient proportion of the genetic variance, then a more relaxed alpha value can be used in the RI screen to increase the statistical power. This flexibility in setting RI alpha values is appropriate only when adequate protection against Type I errors comes from the F-2 (or other) confirmation test(s).
引用
收藏
页码:149 / 160
页数:12
相关论文
共 44 条
[1]
[Anonymous], 1981, Statistical Tables
[2]
BAILEY DW, 1981, MOUSE BIOMEDICAL RES, V1, P223
[3]
LOCALIZATION TO CHROMOSOME-10 OF A LOCUS INFLUENCING MORPHINE ANALGESIA IN CROSSES DERIVED FROM C57BL/6 AND DBA/2 STRAINS [J].
BELKNAP, JK ;
MOGIL, JS ;
HELMS, ML ;
RICHARDS, SP ;
OTOOLE, LA ;
BERGESON, SE ;
BUCK, KJ .
LIFE SCIENCES, 1995, 57 (10) :PL117-PL124
[4]
EMPIRICAL ESTIMATES OF BONFERRONI CORRECTIONS FOR USE IN CHROMOSOME MAPPING STUDIES WITH THE BXD RECOMBINANT INBRED STRAINS [J].
BELKNAP, JK .
BEHAVIOR GENETICS, 1992, 22 (06) :677-684
[5]
BELKNAP JK, 1993, BEHAV GENET, V23, P211
[6]
QUANTITATIVE TRAIT LOCI MAPPING OF 3 LOCI CONTROLLING MORPHINE PREFERENCE USING INBRED MOUSE STRAINS [J].
BERRETTINI, WH ;
FERRARO, TN ;
ALEXANDER, RC ;
BUCHBERG, AM ;
VOGEL, WH .
NATURE GENETICS, 1994, 7 (01) :54-58
[7]
STRATEGIES FOR MAPPING AND IDENTIFYING QUANTITATIVE TRAIT LOCI SPECIFYING BEHAVIORAL-RESPONSES TO ALCOHOL [J].
BUCK, KJ .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1995, 19 (04) :795-801
[8]
GENETIC ANIMAL-MODELS OF ALCOHOL AND DRUG-ABUSE [J].
CRABBE, JC ;
BELKNAP, JK ;
BUCK, KJ .
SCIENCE, 1994, 264 (5166) :1715-1723
[9]
CRABBE JC, 1995, MOL APPROACHES DRUG, V3
[10]
CRABBE JC, 1994, ALCOHOL ALCOHOLISM S, V2, P69