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Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data
The Mouse Phenome Database (MPD; https://phenome.jax.org) is a widely accessed and highly functional data repository housing primary phenotype data for the laboratory mouse accessible via APIs and providing tools to analyze and visualize those data. Data come from investigators around the world and...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145612/ https://www.ncbi.nlm.nih.gov/pubmed/31696236 http://dx.doi.org/10.1093/nar/gkz1032 |
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author | Bogue, Molly A Philip, Vivek M Walton, David O Grubb, Stephen C Dunn, Matthew H Kolishovski, Georgi Emerson, Jake Mukherjee, Gaurab Stearns, Timothy He, Hao Sinha, Vinita Kadakkuzha, Beena Kunde-Ramamoorthy, Govindarajan Chesler, Elissa J |
author_facet | Bogue, Molly A Philip, Vivek M Walton, David O Grubb, Stephen C Dunn, Matthew H Kolishovski, Georgi Emerson, Jake Mukherjee, Gaurab Stearns, Timothy He, Hao Sinha, Vinita Kadakkuzha, Beena Kunde-Ramamoorthy, Govindarajan Chesler, Elissa J |
author_sort | Bogue, Molly A |
collection | PubMed |
description | The Mouse Phenome Database (MPD; https://phenome.jax.org) is a widely accessed and highly functional data repository housing primary phenotype data for the laboratory mouse accessible via APIs and providing tools to analyze and visualize those data. Data come from investigators around the world and represent a broad scope of phenotyping endpoints and disease-related traits in naïve mice and those exposed to drugs, environmental agents or other treatments. MPD houses rigorously curated per-animal data with detailed protocols. Public ontologies and controlled vocabularies are used for annotation. In addition to phenotype tools, genetic analysis tools enable users to integrate and interpret genome–phenome relations across the database. Strain types and populations include inbred, recombinant inbred, F1 hybrid, transgenic, targeted mutants, chromosome substitution, Collaborative Cross, Diversity Outbred and other mapping populations. Our new analysis tools allow users to apply selected data in an integrated fashion to address problems in trait associations, reproducibility, polygenic syndrome model selection and multi-trait modeling. As we refine these tools and approaches, we will continue to provide users a means to identify consistent, quality studies that have high translational relevance. |
format | Online Article Text |
id | pubmed-7145612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71456122020-04-13 Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data Bogue, Molly A Philip, Vivek M Walton, David O Grubb, Stephen C Dunn, Matthew H Kolishovski, Georgi Emerson, Jake Mukherjee, Gaurab Stearns, Timothy He, Hao Sinha, Vinita Kadakkuzha, Beena Kunde-Ramamoorthy, Govindarajan Chesler, Elissa J Nucleic Acids Res Database Issue The Mouse Phenome Database (MPD; https://phenome.jax.org) is a widely accessed and highly functional data repository housing primary phenotype data for the laboratory mouse accessible via APIs and providing tools to analyze and visualize those data. Data come from investigators around the world and represent a broad scope of phenotyping endpoints and disease-related traits in naïve mice and those exposed to drugs, environmental agents or other treatments. MPD houses rigorously curated per-animal data with detailed protocols. Public ontologies and controlled vocabularies are used for annotation. In addition to phenotype tools, genetic analysis tools enable users to integrate and interpret genome–phenome relations across the database. Strain types and populations include inbred, recombinant inbred, F1 hybrid, transgenic, targeted mutants, chromosome substitution, Collaborative Cross, Diversity Outbred and other mapping populations. Our new analysis tools allow users to apply selected data in an integrated fashion to address problems in trait associations, reproducibility, polygenic syndrome model selection and multi-trait modeling. As we refine these tools and approaches, we will continue to provide users a means to identify consistent, quality studies that have high translational relevance. Oxford University Press 2020-01-08 2019-11-07 /pmc/articles/PMC7145612/ /pubmed/31696236 http://dx.doi.org/10.1093/nar/gkz1032 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Database Issue Bogue, Molly A Philip, Vivek M Walton, David O Grubb, Stephen C Dunn, Matthew H Kolishovski, Georgi Emerson, Jake Mukherjee, Gaurab Stearns, Timothy He, Hao Sinha, Vinita Kadakkuzha, Beena Kunde-Ramamoorthy, Govindarajan Chesler, Elissa J Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data |
title | Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data |
title_full | Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data |
title_fullStr | Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data |
title_full_unstemmed | Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data |
title_short | Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data |
title_sort | mouse phenome database: a data repository and analysis suite for curated primary mouse phenotype data |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145612/ https://www.ncbi.nlm.nih.gov/pubmed/31696236 http://dx.doi.org/10.1093/nar/gkz1032 |
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