Evidence map›Paper›PMID 30389793›Full record

ArticleG3 (Bethesda, Md.)2018

Mean-Variance QTL Mapping Identifies Novel QTL for Circadian Activity and Exploratory Behavior in Mice.

Robert W Corty, Vivek Kumar, Lisa M Tarantino, Joseph S Takahashi, William Valdar

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Life science alliance · 2020
    Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Robert W CortyDepartment of Genetics.ORCID 0000-0002-6787-9051
Vivek KumarThe Jackson Laboratory.ORCID 0000-0001-6643-7465
Lisa M TarantinoBioinformatics and Computational Biology Curriculum.ORCID 0000-0001-9984-2600
Joseph S TakahashiHoward Hughes Medical Institute, Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0003-0384-8878
William ValdarDepartment of Genetics william.valdar@unc.edu.ORCID 0000-0002-2419-0430

Funding

Statistical Modeling of Multiparental and Genetic Reference PopulationsR35GM127000 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI William Valdar · 2018 to 2026
$3.1M
Sequencing Mutant Mice With Altered Cocaine ResponsesU01DA041668 · NIDA · JACKSON LABORATORY · PI KUMAR, VIVEK · 2016 to 2020
$2.8M
UNC Predoc Training Progr in Bioinformatics/Comp BiologyT32GM067553 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ELSTON, TIMOTHY C · 2005 to 2019
$2.5M
Statistical Modeling of Complex Traits in Genetic Reference Super-PopulationsR01GM104125 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI VALDAR, WILLIAM · 2012 to 2016
$1.2M
Big Data to Knowledge Training ProgramT32LM012420 · NLM · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FOREST, MARK GREGORY, KOSOROK, MICHAEL R · 2016 to 2019
$1.1M
The interplay between genes and environment on cardiovascular disease phenotypesR21HL126045 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LANGE, ETHAN MATHER, LANGE, LESLIE A · 2015 to 2016
$447k
Statistical modeling of genetic effects on behavior and its variabilityF30MH108265 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CORTY, ROBERT WALLACE · 2016 to 2018
$119k
NHLBI NIH HHS R21 HL126045NIDA NIH HHS U01 DA041668NIGMS NIH HHS R01 GM104125NIGMS NIH HHS R35 GM127000NIGMS NIH HHS T32 GM067553NIMH NIH HHS F30 MH108265NLM NIH HHS T32 LM012420
6 · The paper itself

Abstract

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 linear model 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.

Indexed as

Chromosome MappingCrosses, GeneticExploratory BehaviorQuantitative Trait, HeritableAnimalsCircadian RhythmMiceDGLMmQTLmvQTLvariance heterogeneirtyvQTL

Identifiers

PMID30389793
PMCPMC6288835

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.