TY - JOUR
T1 - Mean-variance QTL mapping identifies novel QTL for circadian activity and exploratory behavior in mice
AU - Corty, Robert W.
AU - Kumar, Vivek
AU - Tarantino, Lisa M.
AU - Takahashi, Joseph S.
AU - Valdar, William
N1 - Funding Information:
This work was funded by National Institutes of General Medical Sciences grants R01-GM104125 (RWC,WV), R35-GM127000 (RWC, WV), T32-GM067553 (RWC); National Heart, Lung and Blood Institute grant R21 HL126045 (RWC,WV); National Library of Medicine grant T32-LM012420 (RWC); and a National Institute of Mental Health grant F30-MH108265 (RWC).
Publisher Copyright:
© 2018 Montesinos-López et al.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - We illustrate, through two case studies, that "mean-variance QTL mapping"-QTL mapping that models effects on the mean and the variance simultaneously-can discover QTL that traditional interval mapping cannot. Mean-variance QTL mapping is based on the double generalized linear model, which extends the standard linearmodel used in interval mapping by incorporating not only a set of genetic and covariate effects for mean but also set of such effects for the residual variance. Its potential for use in QTL mapping has been described previously, but it remains underutilized, with certain key advantages undemonstrated until now. In the first case study, a reduced complexity intercross of C57BL/6J and C57BL/6N mice examining circadian behavior, our reanalysis detected a mean-controlling QTL for circadian wheel running activity that interval mapping did not; mean-variance QTL mapping was more powerful than interval mapping at the QTL because it accounted for the fact that mice homozygous for the C57BL/6N allele had less residual variance than other mice. In the second case study, an intercross between C57BL/6J and C58/J mice examining anxiety-like behaviors, our reanalysis detected a variance-controlling QTL for rearing behavior; interval mapping did not identify this QTL because it does not target variance QTL. We believe that the results of these reanalyses, which in other respects largely replicated the original findings, support the use of mean-variance QTL mapping as standard practice.
AB - We illustrate, through two case studies, that "mean-variance QTL mapping"-QTL mapping that models effects on the mean and the variance simultaneously-can discover QTL that traditional interval mapping cannot. Mean-variance QTL mapping is based on the double generalized linear model, which extends the standard linearmodel used in interval mapping by incorporating not only a set of genetic and covariate effects for mean but also set of such effects for the residual variance. Its potential for use in QTL mapping has been described previously, but it remains underutilized, with certain key advantages undemonstrated until now. In the first case study, a reduced complexity intercross of C57BL/6J and C57BL/6N mice examining circadian behavior, our reanalysis detected a mean-controlling QTL for circadian wheel running activity that interval mapping did not; mean-variance QTL mapping was more powerful than interval mapping at the QTL because it accounted for the fact that mice homozygous for the C57BL/6N allele had less residual variance than other mice. In the second case study, an intercross between C57BL/6J and C58/J mice examining anxiety-like behaviors, our reanalysis detected a variance-controlling QTL for rearing behavior; interval mapping did not identify this QTL because it does not target variance QTL. We believe that the results of these reanalyses, which in other respects largely replicated the original findings, support the use of mean-variance QTL mapping as standard practice.
KW - DGLM
KW - heterogeneirty
KW - mQTL
KW - mvQTL
KW - vQTL
KW - variance
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U2 - 10.1534/g3.118.200194
DO - 10.1534/g3.118.200194
M3 - Article
C2 - 30389793
AN - SCOPUS:85058175182
SN - 2160-1836
VL - 8
SP - 3783
EP - 3790
JO - G3: Genes, Genomes, Genetics
JF - G3: Genes, Genomes, Genetics
IS - 12
ER -