ArticleMammalian genome : official journal of the International Mammalian Genome Society2007
Mouse Phenotype Database Integration Consortium: integration [corrected] of mouse phenome data resources.
Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.
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.
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.
Who cites it
24 citing papers in PubMed.
- Reproducibility and replicability of rodent phenotyping in preclinical studies.Neuroscience and biobehavioral reviews · 2018Review
- The digital revolution in phenotyping.Briefings in bioinformatics · 2016Article
- Article
- Genome-wide association studies in mice.Nature reviews. Genetics · 2012Review
- Three ontologies to define phenotype measurement data.Frontiers in genetics · 2012Article
- Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome.PLoS genetics · 2012Article
- Research resources: curating the new eagle-i discovery system.Database : the journal of biological databases and curation · 2012Article
- Strategies and methods to study sex differences in cardiovascular structure and function: a guide for basic scientists.Biology of sex differences · 2011Article
- Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia.Nature genetics · 2011Article
- Mouse models in male fertility research.Asian journal of andrology · 2011Review
- The RIKEN integrated database of mammals.Nucleic acids research · 2011Article
- Meeting Report from the Second "Minimum Information for Biological and Biomedical Investigations" (MIBBI) workshop.Standards in genomic sciences · 2010Article
- A MOD(ern) perspective on literature curation.Molecular genetics and genomics : MGG · 2010Article
- SDOP-DB: a comparative standardized-protocol database for mouse phenotypic analyses.Bioinformatics (Oxford, England) · 2010Article
- Systematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic information.BMC medical genomics · 2010Article
- MouseBook: an integrated portal of mouse resources.Nucleic acids research · 2010Article
- Where's the mouse info?Veterinary pathology · 2009Article
- Mouse, man, and meaning: bridging the semantics of mouse phenotype and human disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2009Article
- Towards better mouse models: enhanced genotypes, systemic phenotyping and envirotype modelling.Nature reviews. Genetics · 2009Review
- Mouse phenome database.Nucleic acids research · 2009Article
Corrections and comments
- Erratum issued
- Erratum issuedmultiple author names added
Authors and funding
38 authors.
Funding
Abstract
Understanding the functions encoded in the mouse genome will be central to an understanding of the genetic basis of human disease. To achieve this it will be essential to be able to characterize the phenotypic consequences of variation and alterations in individual genes. Data on the phenotypes of mouse strains are currently held in a number of different forms (detailed descriptions of mouse lines, first-line phenotyping data on novel mutations, data on the normal features of inbred lines) at many sites worldwide. For the most efficient use of these data sets, we have initiated a process to develop standards for the description of phenotypes (using ontologies) and file formats for the description of phenotyping protocols and phenotype data sets. This process is ongoing and needs to be supported by the wider mouse genetics and phenotyping communities to succeed. We invite interested parties to contact us as we develop this process further.
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What OpenQuestion holds
Registered trials
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 OpenQuestion graph.