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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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.
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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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